A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv592509



Internal ID16379918
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:172013271..172037453hg38UCSC Ensembl
Innerchr3:171731061..171755243hg19UCSC Ensembl
Innerchr3:173213755..173237937hg18UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg3824183
hg1924183
hg1824183
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv981215
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv592509
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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