A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3688933



Internal ID18640528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:39053783..39314111hg38UCSC Ensembl
Innerchr9:39053780..39314108hg19UCSC Ensembl
Innerchr9:39043780..39304108hg18UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg38260329
hg19260329
hg18260329
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1018060
Supporting Variants
Samples
Known GenesCNTNAP3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3688933
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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