A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614082



Internal ID16401491
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:29986252..30053822hg38UCSC Ensembl
Innerchr9:29986250..30053820hg19UCSC Ensembl
Innerchr9:29976250..30043820hg18UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg3867571
hg1967571
hg1867571
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12645n54
Supporting Variantsnssv1156767
Samples1780862574_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614082
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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