A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700711



Internal ID15437363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:125876345..125883032hg38UCSC Ensembl
Innerchr8:126888589..126895276hg19UCSC Ensembl
Innerchr8:126957771..126964458hg18UCSC Ensembl
Innerchr8:126957771..126964458hg17UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg386688
hg196688
hg186688
hg176688
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524724
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700711
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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