A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv584039



Internal ID16371448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:187570916..187618206hg38UCSC Ensembl
Innerchr2:188435643..188482933hg19UCSC Ensembl
Innerchr2:188143888..188191178hg18UCSC Ensembl
Cytoband2q32.1
Allele length
AssemblyAllele length
hg3847291
hg1947291
hg1847291
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv928245
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv584039
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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