A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623561



Internal ID7010417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:65276805..65291171hg38UCSC Ensembl
Innerchr10:65277305..65290671hg38UCSC Ensembl
Outerchr10:65275805..65292171hg38UCSC Ensembl
chr10:67036563..67050929hg19UCSC Ensembl
Innerchr10:67037063..67050429hg19UCSC Ensembl
Outerchr10:67035563..67051929hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg3814367
hg1914367
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13839475, essv13839474, essv13839476
SamplesHG01486, NA19475, NA19316
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623561
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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