A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv616012



Internal ID16403421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:137197680..137223834hg38UCSC Ensembl
Innerchr9:140092132..140118286hg19UCSC Ensembl
Innerchr9:139211953..139238107hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3826155
hg1926155
hg1826155
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1148366
Samples
Known GenesNDOR1, RNF208, TMEM203, TPRN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv616012
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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