A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3598102



Internal ID6985238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:146709659..146710502hg38UCSC Ensembl
Innerchr3:146709659..146710502hg38UCSC Ensembl
Outerchr3:146709383..146710771hg38UCSC Ensembl
chr3:146427446..146428289hg19UCSC Ensembl
Innerchr3:146427446..146428289hg19UCSC Ensembl
Outerchr3:146427170..146428558hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg38844
hg19844
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11176260, essv11176243, essv11176245, essv11176253, essv11176269, essv11176240, essv11176263, essv11176258, essv11176241, essv11176247, essv11176266, essv11176257, essv11176264, essv11176236, essv11176251, essv11176242, essv11176256, essv11176238, essv11176244, essv11176246, essv11176261, essv11176248, essv11176237, essv11176255, essv11176254, essv11176267, essv11176270, essv11176239, essv11176265, essv11176259, essv11176268, essv11176249, essv11176262, essv11176252, essv11176250
SamplesNA19703, NA19704, NA18504, HG02769, NA19171, NA19197, HG01365, HG02505, HG03212, NA19901, HG01048, HG03270, HG03120, NA20536, NA19391, NA18516, HG02953, HG01941, HG02470, HG01889, HG03294, NA18907, HG03382, NA19452, HG01890, NA19225, HG02330, NA19256, NA19435, HG03103, HG03084, NA19472, HG03063, HG02768, HG03265
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3598102
Frequency
Sample Size2504
Observed Gain0
Observed Loss35
Observed Complex0
Frequencyn/a


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