A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3585744



Internal ID6973265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:37056268..37057103hg38UCSC Ensembl
Innerchr1:37056268..37057103hg38UCSC Ensembl
Outerchr1:37055932..37057387hg38UCSC Ensembl
chr1:37521869..37522704hg19UCSC Ensembl
Innerchr1:37521869..37522704hg19UCSC Ensembl
Outerchr1:37521533..37522988hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg38836
hg19836
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9908796, essv9908799, essv9908792, essv9908802, essv9908801, essv9908800, essv9908803, essv9908785, essv9908788, essv9908786, essv9908795, essv9908783, essv9908784, essv9908789, essv9908793, essv9908791, essv9908794, essv9908787, essv9908797, essv9908798, essv9908790
SamplesHG01412, NA19332, HG02012, HG00640, HG03190, NA20346, HG03069, NA19917, NA19445, NA18908, HG03120, NA19455, HG02108, HG01204, NA19375, HG02455, HG03259, HG03469, HG03432, NA19351, NA19153
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3585744
Frequency
Sample Size2504
Observed Gain0
Observed Loss21
Observed Complex0
Frequencyn/a


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