A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1173838



Internal ID15874559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:41699460..41732905hg38UCSC Ensembl
Innerchr1:42165131..42198576hg19UCSC Ensembl
Innerchr1:41937718..41971163hg18UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg3833446
hg1933446
hg1833446
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv546109
Supporting Variants
SamplesHGDP00553
Known GenesHIVEP3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1173838
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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