A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1151795



Internal ID15873856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:127667659..127702011hg38UCSC Ensembl
Innerchr3:127386502..127420854hg19UCSC Ensembl
Innerchr3:128869192..128903544hg18UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg3834353
hg1934353
hg1834353
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv591585
Supporting Variants
SamplesHGDP00402
Known GenesABTB1, MGLL, PODXL2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1151795
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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