A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700974



Internal ID15437626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:28218754..28267762hg38UCSC Ensembl
Innerchr8:28076271..28125279hg19UCSC Ensembl
Innerchr8:28132190..28181198hg18UCSC Ensembl
Innerchr8:28132190..28181198hg17UCSC Ensembl
Cytoband8p21.1
Allele length
AssemblyAllele length
hg3849009
hg1949009
hg1849009
hg1749009
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524953
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700974
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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