A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3570713



Internal ID6695409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:1438833..1438968hg38UCSC Ensembl
chr10:1481028..1481163hg19UCSC Ensembl
chr10:1471028..1471163hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38136
hg19136
hg18136
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv998745
Supporting Variants
SamplesHuRef
Known GenesADARB2
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3570713
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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