A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv709662



Internal ID15656932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:9258342..9352728hg38UCSC Ensembl
Innerchr1:9318401..9412787hg19UCSC Ensembl
Innerchr1:9240988..9335374hg18UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg3894387
hg1994387
hg1894387
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv545356
Supporting Variants
Samples
Known GenesH6PD, SPSB1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv709662
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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