A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623699



Internal ID7010555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:68001317..68002444hg38UCSC Ensembl
Innerchr10:68001367..68002394hg38UCSC Ensembl
Outerchr10:68001267..68002494hg38UCSC Ensembl
chr10:69761074..69762201hg19UCSC Ensembl
Innerchr10:69761124..69762151hg19UCSC Ensembl
Outerchr10:69761024..69762251hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg381128
hg191128
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13848638, essv13848637
SamplesNA20521, HG01131
Known GenesHERC4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623699
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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