A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3697507



Internal ID18995788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:77157412..77171286hg38UCSC Ensembl
Innerchr9:79772328..79786202hg19UCSC Ensembl
Innerchr9:78962148..78976022hg18UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg3813875
hg1913875
hg1813875
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1036385
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3697507
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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