A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3692388



Internal ID18990669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:4291268..4384038hg38UCSC Ensembl
Innerchr9:4291268..4384038hg19UCSC Ensembl
Innerchr9:4281268..4374038hg18UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg3892771
hg1992771
hg1892771
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1023363
Supporting Variants
Samples
Known GenesGLIS3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3692388
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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