A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv686032



Internal ID15422684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:245152917..245164783hg38UCSC Ensembl
Innerchr1:245316219..245328085hg19UCSC Ensembl
Innerchr1:243382842..243394708hg18UCSC Ensembl
Innerchr1:241642260..241654126hg17UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg3811867
hg1911867
hg1811867
hg1711867
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515634
Supporting Variants
Samples
Known GenesKIF26B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv686032
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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