A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615248



Internal ID16402657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:114458493..114460395hg38UCSC Ensembl
Innerchr9:117220773..117222675hg19UCSC Ensembl
Innerchr9:116260594..116262496hg18UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg381903
hg191903
hg181903
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1141278
Samples
Known GenesDFNB31
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615248
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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