A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614563



Internal ID16401972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:69280692..69284053hg38UCSC Ensembl
Innerchr9:71895608..71898969hg19UCSC Ensembl
Innerchr9:71085428..71088789hg18UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg383362
hg193362
hg183362
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12742n54
Supporting Variantsnssv1137093, nssv1137097, nssv1137096, nssv1137086, nssv1137094, nssv1137091, nssv1137092, nssv1137089, nssv1137090, nssv1137087, nssv1137095, nssv1137088
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614563
Frequency
Sample Size17421
Observed Gain0
Observed Loss12
Observed Complex0
Frequencyn/a


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