A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614185



Internal ID16401594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:36310645..36456546hg38UCSC Ensembl
Innerchr9:36310642..36456543hg19UCSC Ensembl
Innerchr9:36300642..36446543hg18UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg38145902
hg19145902
hg18145902
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1132980
Samples
Known GenesRNF38
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614185
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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