A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590046



Internal ID16377455
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:32297503..32302814hg38UCSC Ensembl
Innerchr3:32338995..32344306hg19UCSC Ensembl
Innerchr3:32313999..32319310hg18UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg385312
hg195312
hg185312
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv962089, nssv962090, nssv962088
Samples
Known GenesCMTM8
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590046
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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