A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv975222



Internal ID16269178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:144057254..144143508hg38UCSC Ensembl
Innerchr3:143776096..143862350hg19UCSC Ensembl
Innerchr3:145258786..145345040hg18UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg3886255
hg1986255
hg1886255
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv591923
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv975222
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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