A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3604726



Internal ID6991754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:36751304..36751902hg38UCSC Ensembl
Innerchr5:36751305..36751901hg38UCSC Ensembl
Outerchr5:36751303..36751903hg38UCSC Ensembl
chr5:36751406..36752004hg19UCSC Ensembl
Innerchr5:36751407..36752003hg19UCSC Ensembl
Outerchr5:36751405..36752005hg19UCSC Ensembl
Cytoband5p13.2
Allele length
AssemblyAllele length
hg38599
hg19599
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11868744, essv11868752, essv11868718, essv11868723, essv11868750, essv11868742, essv11868730, essv11868743, essv11868753, essv11868733, essv11868735, essv11868749, essv11868725, essv11868731, essv11868736, essv11868747, essv11868739, essv11868740, essv11868748, essv11868721, essv11868746, essv11868754, essv11868724, essv11868734, essv11868726, essv11868745, essv11868732, essv11868727, essv11868722, essv11868729, essv11868728, essv11868741, essv11868717, essv11868751, essv11868755, essv11868738, essv11868737, essv11868719, essv11868720, essv11868756
SamplesNA19332, HG02702, HG03175, NA19092, NA18486, HG03190, HG03295, NA19098, HG03095, NA19374, HG03436, HG02054, NA19038, NA19923, HG02315, HG03268, NA19372, NA19027, HG02819, HG03132, NA19403, HG02449, HG02968, HG02309, HG02881, HG03567, HG02557, HG02799, NA19434, HG02837, NA19310, HG01108, HG03419, HG02771, HG02974, HG03258, NA20289, NA19116, HG03198, HG03166
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3604726
Frequency
Sample Size2504
Observed Gain0
Observed Loss40
Observed Complex0
Frequencyn/a


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