A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611153



Internal ID6998064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:146450703..146456370hg38UCSC Ensembl
Innerchr6:146450753..146456320hg38UCSC Ensembl
Outerchr6:146450587..146456486hg38UCSC Ensembl
chr6:146771839..146777506hg19UCSC Ensembl
Innerchr6:146771889..146777456hg19UCSC Ensembl
Outerchr6:146771723..146777622hg19UCSC Ensembl
Cytoband6q24.3
Allele length
AssemblyAllele length
hg385668
hg195668
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12577165, essv12577186, essv12577129, essv12577139, essv12577162, essv12577144, essv12577175, essv12577124, essv12577198, essv12577166, essv12577194, essv12577158, essv12577190, essv12577118, essv12577161, essv12577155, essv12577126, essv12577125, essv12577163, essv12577199, essv12577171, essv12577184, essv12577132, essv12577140, essv12577172, essv12577130, essv12577145, essv12577149, essv12577152, essv12577138, essv12577136, essv12577176, essv12577193, essv12577119, essv12577181, essv12577153, essv12577121, essv12577177, essv12577156, essv12577120, essv12577189, essv12577151, essv12577191, essv12577179, essv12577180, essv12577134, essv12577168, essv12577128, essv12577192, essv12577173, essv12577164, essv12577148, essv12577200, essv12577157, essv12577137, essv12577196, essv12577133, essv12577146, essv12577188, essv12577122, essv12577182, essv12577169, essv12577174, essv12577154, essv12577116, essv12577127, essv12577167, essv12577123, essv12577147, essv12577141, essv12577183, essv12577197, essv12577142, essv12577159, essv12577178, essv12577117, essv12577150, essv12577135, essv12577187, essv12577185, essv12577160, essv12577170, essv12577195, essv12577143, essv12577131
SamplesHG02890, HG02628, NA19397, NA18924, NA19909, HG01885, NA19914, HG03517, HG03241, HG02419, NA19350, HG02804, HG02323, HG03521, NA20294, NA20298, HG01518, HG03139, HG02895, HG02769, NA19319, HG02811, NA19315, HG02952, HG03342, HG02645, NA19038, HG02505, NA19922, HG02634, HG02461, NA19385, NA19317, NA19159, NA19026, HG02427, HG03058, NA19456, HG03114, HG02678, NA19455, HG02108, HG02307, NA18910, HG03159, HG02757, HG02309, HG03391, NA18523, HG02332, HG02586, HG02896, HG02594, NA18858, NA19035, HG01992, NA19308, HG03028, HG02667, NA19390, NA19147, HG02799, NA19712, HG02308, HG01131, HG02721, NA19435, NA19380, NA19144, NA19467, HG02580, NA19360, NA19475, NA19818, HG03565, HG02970, HG03066, HG02053, NA19096, NA19900, NA19129, NA18511, HG02643, HG00554, HG02760
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611153
Frequency
Sample Size2504
Observed Gain0
Observed Loss85
Observed Complex0
Frequencyn/a


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