A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615516



Internal ID16402925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:130268828..130271833hg38UCSC Ensembl
Innerchr9:133031107..133034112hg19UCSC Ensembl
Innerchr9:132070928..132073933hg18UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg383006
hg193006
hg183006
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12909n54
Supporting Variantsnssv1145179, nssv1145180
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615516
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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