A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv686755



Internal ID15076721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:167191722..167388324hg38UCSC Ensembl
Innerchr1:167160959..167357561hg19UCSC Ensembl
Innerchr1:165427583..165624185hg18UCSC Ensembl
Innerchr1:163892617..164089219hg17UCSC Ensembl
Cytoband1q24.1
Allele length
AssemblyAllele length
hg38196603
hg19196603
hg18196603
hg17196603
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521232
Supporting Variants
Samples
Known GenesPOU2F1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv686755
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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