A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv581979



Internal ID16369388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:52989779..53060928hg38UCSC Ensembl
Innerchr2:53216917..53288066hg19UCSC Ensembl
Innerchr2:53070421..53141570hg18UCSC Ensembl
Cytoband2p16.2
Allele length
AssemblyAllele length
hg3871150
hg1971150
hg1871150
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6887n54
Supporting Variantsnssv909350
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv581979
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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