A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615513



Internal ID16402922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:130268588..130272119hg38UCSC Ensembl
Innerchr9:133030867..133034398hg19UCSC Ensembl
Innerchr9:132070688..132074219hg18UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg383532
hg193532
hg183532
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12909n54
Supporting Variantsnssv1145175
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615513
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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