A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614422



Internal ID16401831
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:43659129..43772166hg19UCSC Ensembl
Innerchr9:43599125..43712162hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg19113038
hg18113038
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12716n54
Supporting Variantsnssv1134444, nssv1134447, nssv1134446, nssv1134445
Samples
Known GenesCNTNAP3B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614422
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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