A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3587734



Internal ID6628035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:161620485..161628311hg38UCSC Ensembl
Innerchr1:161620485..161628311hg38UCSC Ensembl
Outerchr1:161620315..161628472hg38UCSC Ensembl
chr1:161590275..161598101hg19UCSC Ensembl
Innerchr1:161590275..161598101hg19UCSC Ensembl
Outerchr1:161590105..161598262hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg387827
hg197827
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10169170, essv10169169, essv10169168, essv10169161, essv10169175, essv10169188, essv10169165, essv10169180, essv10169176, essv10169182, essv10169185, essv10169172, essv10169160, essv10169174, essv10169164, essv10169189, essv10169171, essv10169187, essv10169167, essv10169184, essv10169181, essv10169186, essv10169179, essv10169162, essv10169166, essv10169177, essv10169173, essv10169178, essv10169183, essv10169163
SamplesHG01359, NA19914, NA19332, NA18596, NA18504, HG02589, HG01522, HG03722, HG03499, NA19678, HG02620, NA19922, NA19372, HG03624, HG02537, NA20867, NA18912, HG03446, NA19035, HG00476, NA19147, HG02049, NA19072, HG02462, HG03684, NA19102, HG03410, NA18984, NA19316, HG03265
Known GenesFCGR3B
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3587734
Frequency
Sample Size2504
Observed Gain0
Observed Loss30
Observed Complex0
Frequencyn/a


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