A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591064



Internal ID16378473
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:98212261..98239436hg38UCSC Ensembl
Innerchr3:97931105..97958280hg19UCSC Ensembl
Innerchr3:99413795..99440970hg18UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg3827176
hg1927176
hg1827176
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8458n54
Supporting Variantsnssv968217
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591064
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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