A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695201



Internal ID15431853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:11132282..11143509hg38UCSC Ensembl
Innerchr17:11035599..11046826hg19UCSC Ensembl
Innerchr17:10976324..10987551hg18UCSC Ensembl
Innerchr17:10976324..10987551hg17UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3811228
hg1911228
hg1811228
hg1711228
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517798
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695201
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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