A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590426



Internal ID16377835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:61370576..61420153hg38UCSC Ensembl
Innerchr3:61356250..61405827hg19UCSC Ensembl
Innerchr3:61331290..61380867hg18UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg3849578
hg1949578
hg1849578
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv963499, nssv963500
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590426
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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