A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590807



Internal ID16378216
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:83045595..83195095hg38UCSC Ensembl
Innerchr3:83094746..83244246hg19UCSC Ensembl
Innerchr3:83177436..83326936hg18UCSC Ensembl
Cytoband3p12.2
Allele length
AssemblyAllele length
hg38149501
hg19149501
hg18149501
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv967069
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590807
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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