A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3690652



Internal ID18988933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:17585689..17632545hg38UCSC Ensembl
Innerchr9:17585687..17632543hg19UCSC Ensembl
Innerchr9:17575687..17622543hg18UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg3846857
hg1946857
hg1846857
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1029253
Supporting Variants
Samples
Known GenesSH3GL2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3690652
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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