A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589814



Internal ID16030537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:16165768..16193535hg38UCSC Ensembl
Innerchr3:16207275..16235042hg19UCSC Ensembl
Innerchr3:16182279..16210046hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3827768
hg1927768
hg1827768
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv959675
Samples
Known GenesGALNT15
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589814
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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