A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv584521



Internal ID16371930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:222992836..223004283hg38UCSC Ensembl
Innerchr2:223857554..223869001hg19UCSC Ensembl
Innerchr2:223565798..223577245hg18UCSC Ensembl
Cytoband2q36.1
Allele length
AssemblyAllele length
hg3811448
hg1911448
hg1811448
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7302n54
Supporting Variantsnssv932446
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv584521
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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