A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3690655



Internal ID18988936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:17585689..17633298hg38UCSC Ensembl
Innerchr9:17585687..17633296hg19UCSC Ensembl
Innerchr9:17575687..17623296hg18UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg3847610
hg1947610
hg1847610
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1032604
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)nssv3690655
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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