A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13864511



Internal ID3866327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:76353972..76356616hg38UCSC Ensembl
Innerchr10:76353972..76356616hg38UCSC Ensembl
Outerchr10:76353748..76356815hg38UCSC Ensembl
chr10:78113730..78116374hg19UCSC Ensembl
Innerchr10:78113730..78116374hg19UCSC Ensembl
Outerchr10:78113506..78116573hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg382645
hg192645
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3623865
Supporting Variants
SamplesHG00559
Known GenesC10orf11
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13864511
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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