A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591363



Internal ID16032086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:119597981..119627103hg38UCSC Ensembl
Innerchr3:119316828..119345950hg19UCSC Ensembl
Innerchr3:120799518..120828640hg18UCSC Ensembl
Cytoband3q13.33
Allele length
AssemblyAllele length
hg3829123
hg1929123
hg1829123
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv971663
Samples
Known GenesPLA1A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591363
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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