A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv672798



Internal ID15409450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:17583312..17630648hg38UCSC Ensembl
Innerchr9:17583310..17630646hg19UCSC Ensembl
Innerchr9:17573310..17620646hg18UCSC Ensembl
Innerchr9:17573310..17620646hg17UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg3847337
hg1947337
hg1847337
hg1747337
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)nssv672798
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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