A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv661211



Internal ID15051177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:12034084..12040700hg38UCSC Ensembl
Innerchr8:11891593..11898209hg19UCSC Ensembl
Innerchr8:11929002..11935618hg18UCSC Ensembl
Innerchr8:11929002..11935618hg17UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg386617
hg196617
hg186617
hg176617
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516685
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv661211
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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