A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv681147



Internal ID15071113
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:113356672..113375733hg38UCSC Ensembl
Innerchr9:116118952..116138013hg19UCSC Ensembl
Innerchr9:115158773..115177834hg18UCSC Ensembl
Innerchr9:113198506..113217567hg17UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3819062
hg1919062
hg1819062
hg1719062
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519849
Supporting Variants
Samples
Known GenesBSPRY, HDHD3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv681147
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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