A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3693007



Internal ID18991288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:42697890..42856259hg38UCSC Ensembl
Innerchr9:44114860..44273229hg19UCSC Ensembl
Innerchr9:44054856..44213225hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg38158370
hg19158370
hg18158370
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1018117
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)nssv3693007
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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