A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591967



Internal ID16379376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:147171868..147247041hg38UCSC Ensembl
Innerchr3:146889655..146964828hg19UCSC Ensembl
Innerchr3:148372345..148447518hg18UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg3875174
hg1975174
hg1875174
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8634n54
Supporting Variantsnssv976379
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591967
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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