A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613671



Internal ID16401080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:16792352..16804084hg38UCSC Ensembl
Innerchr9:16792350..16804082hg19UCSC Ensembl
Innerchr9:16782350..16794082hg18UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg3811733
hg1911733
hg1811733
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1129287
Samples
Known GenesBNC2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613671
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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