A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1134461



Internal ID15987647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:67043898..67134080hg38UCSC Ensembl
Innerchr9:43669753..43760993hg19UCSC Ensembl
Innerchr9:43609749..43700989hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3890183
hg1991241
hg1891241
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv614427
Supporting Variants
Samples
Known GenesCNTNAP3B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1134461
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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