A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591927



Internal ID16379336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:144279685..144335844hg38UCSC Ensembl
Innerchr3:143998527..144054686hg19UCSC Ensembl
Innerchr3:145481217..145537376hg18UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg3856160
hg1956160
hg1856160
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv975227, nssv975226
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591927
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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