A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1173863



Internal ID15872708
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:25364088..25404497hg38UCSC Ensembl
Innerchr10:25653017..25693426hg19UCSC Ensembl
Innerchr10:25693023..25733432hg18UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3840410
hg1940410
hg1840410
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv550226
Supporting Variants
SamplesHGDP00019
Known GenesGPR158
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1173863
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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