A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614651



Internal ID16402060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:73404629..73411757hg38UCSC Ensembl
Innerchr9:76019545..76026673hg19UCSC Ensembl
Innerchr9:75209365..75216493hg18UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg387129
hg197129
hg187129
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12756n54
Supporting Variantsnssv1137314, nssv1137315
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614651
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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