A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3696413



Internal ID18648008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:134261330..134450961hg38UCSC Ensembl
Innerchr9:137153176..137342807hg19UCSC Ensembl
Innerchr9:136292997..136482628hg18UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg38189632
hg19189632
hg18189632
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1054219
Supporting Variants
Samples
Known GenesMIR4669, RXRA
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3696413
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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