A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13695992



Internal ID1030901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:11641995..11651584hg38UCSC Ensembl
Innerchr10:11641995..11651584hg38UCSC Ensembl
Outerchr10:11641495..11652084hg38UCSC Ensembl
chr10:11683994..11693583hg19UCSC Ensembl
Innerchr10:11683994..11693583hg19UCSC Ensembl
Outerchr10:11683494..11694083hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg389590
hg199590
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622342
Supporting Variants
SamplesHG00653
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13695992
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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