A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3690665



Internal ID18988946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:17590301..17636676hg38UCSC Ensembl
Innerchr9:17590299..17636674hg19UCSC Ensembl
Innerchr9:17580299..17626674hg18UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg3846376
hg1946376
hg1846376
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1031193
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)nssv3690665
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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