A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1134078



Internal ID15640578
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 StatusS
Merged Variantsnsv614283
Supporting Variants
Samples
Known GenesCNTNAP3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1134078
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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