A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623791



Internal ID6663958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:72100628..72103478hg38UCSC Ensembl
Innerchr10:72100642..72103464hg38UCSC Ensembl
Outerchr10:72100614..72103492hg38UCSC Ensembl
chr10:73860386..73863236hg19UCSC Ensembl
Innerchr10:73860400..73863222hg19UCSC Ensembl
Outerchr10:73860372..73863250hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg382851
hg192851
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13861559, essv13861556, essv13861558, essv13861560, essv13861561, essv13861555, essv13861557
SamplesHG02325, NA19916, NA19197, NA19024, HG03583, HG01205, NA19818
Known GenesASCC1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623791
Frequency
Sample Size2504
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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