A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615506



Internal ID16402915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:130268472..130271313hg38UCSC Ensembl
Innerchr9:133030751..133033592hg19UCSC Ensembl
Innerchr9:132070572..132073413hg18UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg382842
hg192842
hg182842
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12909n54
Supporting Variantsnssv1145122, nssv1145120, nssv1145121
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615506
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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