A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv581496



Internal ID16368905
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:39854914..39896764hg38UCSC Ensembl
Innerchr2:40082054..40123904hg19UCSC Ensembl
Innerchr2:39935558..39977408hg18UCSC Ensembl
Cytoband2p22.1
Allele length
AssemblyAllele length
hg3841851
hg1941851
hg1841851
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv906888
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv581496
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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