A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3696221



Internal ID18647816
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:68963578..69228107hg38UCSC Ensembl
Innerchr9:71578494..71843023hg19UCSC Ensembl
Innerchr9:70768314..71032843hg18UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg38264530
hg19264530
hg18264530
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1050692
Supporting Variants
Samples
Known GenesFXN, PIP5K1B, PRKACG, TJP2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3696221
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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