A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614142



Internal ID16401551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:32224468..32283646hg38UCSC Ensembl
Innerchr9:32224466..32283644hg19UCSC Ensembl
Innerchr9:32214466..32273644hg18UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg3859179
hg1959179
hg1859179
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1176061
SamplesHGDP00687
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614142
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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