A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv998236



Internal ID19157773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:22938141..22969861hg38UCSC Ensembl
Innerchr3:22979632..23011352hg19UCSC Ensembl
Innerchr3:22954636..22986356hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3831721
hg1931721
hg1831721
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3589492
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv998236
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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