A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv675357



Internal ID15412009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:17583312..17631554hg38UCSC Ensembl
Innerchr9:17583310..17631552hg19UCSC Ensembl
Innerchr9:17573310..17621552hg18UCSC Ensembl
Innerchr9:17573310..17621552hg17UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg3848243
hg1948243
hg1848243
hg1748243
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517380
Supporting Variants
Samples
Known GenesSH3GL2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv675357
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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