A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700608



Internal ID15090574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:245152917..245173470hg38UCSC Ensembl
Innerchr1:245316219..245336772hg19UCSC Ensembl
Innerchr1:243382842..243403395hg18UCSC Ensembl
Innerchr1:241642260..241662813hg17UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg3820554
hg1920554
hg1820554
hg1720554
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524642
Supporting Variants
Samples
Known GenesKIF26B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700608
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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