A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv583669



Internal ID16371078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:175723305..175757198hg38UCSC Ensembl
Innerchr2:176588033..176621926hg19UCSC Ensembl
Innerchr2:176296279..176330172hg18UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg3833894
hg1933894
hg1833894
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv925611
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv583669
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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