A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13749627



Internal ID6823672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:31562936..31578541hg38UCSC Ensembl
Innerchr10:31562973..31578505hg38UCSC Ensembl
Outerchr10:31562900..31578578hg38UCSC Ensembl
chr10:31851864..31867469hg19UCSC Ensembl
Innerchr10:31851901..31867433hg19UCSC Ensembl
Outerchr10:31851828..31867506hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg3815606
hg1915606
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622813
Supporting Variants
SamplesNA20901
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13749627
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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