A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv584092



Internal ID16371501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:194311489..194395007hg38UCSC Ensembl
Innerchr2:195176213..195259731hg19UCSC Ensembl
Innerchr2:194884458..194967976hg18UCSC Ensembl
Cytoband2q32.3
Allele length
AssemblyAllele length
hg3883519
hg1983519
hg1883519
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7238n54
Supporting Variantsnssv1151120
SamplesHGDP00144
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv584092
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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