A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615509



Internal ID16402918
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:130268472..130271833hg38UCSC Ensembl
Innerchr9:133030751..133034112hg19UCSC Ensembl
Innerchr9:132070572..132073933hg18UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg383362
hg193362
hg183362
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12909n54
Supporting Variantsnssv1145126, nssv1145128, nssv1145127
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615509
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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