A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv583239



Internal ID16370648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:142151616..142206407hg38UCSC Ensembl
Innerchr2:142909185..142963976hg19UCSC Ensembl
Innerchr2:142625655..142680446hg18UCSC Ensembl
Cytoband2q22.2
Allele length
AssemblyAllele length
hg3854792
hg1954792
hg1854792
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1151321
SamplesNINDS_241
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv583239
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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