A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13707111



Internal ID1993620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:17567393..17585156hg38UCSC Ensembl
Innerchr10:17567393..17585156hg38UCSC Ensembl
Outerchr10:17566893..17585656hg38UCSC Ensembl
chr10:17609392..17627155hg19UCSC Ensembl
Innerchr10:17609392..17627155hg19UCSC Ensembl
Outerchr10:17608892..17627655hg19UCSC Ensembl
Cytoband10p12.33
Allele length
AssemblyAllele length
hg3817764
hg1917764
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622491
Supporting Variants
SamplesHG01848
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13707111
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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