A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3692362



Internal ID18990643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:2508296..2575408hg38UCSC Ensembl
Innerchr9:2508296..2575408hg19UCSC Ensembl
Innerchr9:2498296..2565408hg18UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg3867113
hg1967113
hg1867113
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1033424
Supporting Variants
Samples
Known GenesFLJ35024
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3692362
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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