A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv725010



Internal ID15672280
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:158695182..158750398hg38UCSC Ensembl
Innerchr1:158664972..158720188hg19UCSC Ensembl
Innerchr1:156931596..156986812hg18UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg3855217
hg1955217
hg1855217
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv547987
Supporting Variants
Samples
Known GenesOR6K2, OR6K3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv725010
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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