A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv582091



Internal ID16369500
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:57380314..57447445hg38UCSC Ensembl
Innerchr2:57607449..57674580hg19UCSC Ensembl
Innerchr2:57460953..57528084hg18UCSC Ensembl
Cytoband2p16.1
Allele length
AssemblyAllele length
hg3867132
hg1967132
hg1867132
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6903n54
Supporting Variantsnssv1150457
Samples1780854219_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv582091
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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