A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13960022



Internal ID6727268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:123122968..123124533hg38UCSC Ensembl
Innerchr10:123122976..123124525hg38UCSC Ensembl
Outerchr10:123122960..123124541hg38UCSC Ensembl
chr10:124882484..124884049hg19UCSC Ensembl
Innerchr10:124882492..124884041hg19UCSC Ensembl
Outerchr10:124882476..124884057hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg381566
hg191566
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624792
Supporting Variants
SamplesNA20853
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13960022
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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