A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv593070



Internal ID16380479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:196127408..196197332hg38UCSC Ensembl
Innerchr3:195854279..195924203hg19UCSC Ensembl
Innerchr3:197338676..197408600hg18UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg3869925
hg1969925
hg1869925
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv986887
Samples
Known GenesLINC00885
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv593070
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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