A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv592521



Internal ID16033244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:172734475..172831848hg38UCSC Ensembl
Innerchr3:172452265..172549638hg19UCSC Ensembl
Innerchr3:173934959..174032332hg18UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg3897374
hg1997374
hg1897374
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8731n54
Supporting Variantsnssv981236, nssv981235
Samples
Known GenesECT2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv592521
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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