A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614283



Internal ID16055006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:39004143..39280719hg38UCSC Ensembl
Innerchr9:39004140..39280716hg19UCSC Ensembl
Innerchr9:38994140..39270716hg18UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg38276577
hg19276577
hg18276577
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1134078
Samples
Known GenesCNTNAP3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614283
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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