A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3692363



Internal ID18643958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:2526760..2633562hg38UCSC Ensembl
Innerchr9:2526760..2633562hg19UCSC Ensembl
Innerchr9:2516760..2623562hg18UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg38106803
hg19106803
hg18106803
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1029876
Supporting Variants
Samples
Known GenesFLJ35024, VLDLR
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3692363
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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