A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591679



Internal ID16032402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:129961523..129990509hg38UCSC Ensembl
Innerchr3:129680366..129709352hg19UCSC Ensembl
Innerchr3:131163056..131192042hg18UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg3828987
hg1928987
hg1828987
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1151797
SamplesHGDP01071
Known GenesTRH
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591679
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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