A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1152276



Internal ID15853278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:147493190..147568125hg38UCSC Ensembl
Innerchr3:147210977..147285912hg19UCSC Ensembl
Innerchr3:148693667..148768602hg18UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg3874936
hg1974936
hg1874936
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv591968
Supporting Variants
Samples1780854061_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1152276
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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