A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv970923



Internal ID16264879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:103378433..103542134hg38UCSC Ensembl
Innerchr3:103097277..103260978hg19UCSC Ensembl
Innerchr3:104579967..104743668hg18UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg38163702
hg19163702
hg18163702
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv591196
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)nssv970923
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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