A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1012124



Internal ID19101342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:165541222..165571868hg38UCSC Ensembl
Innerchr3:165259010..165289656hg19UCSC Ensembl
Innerchr3:166741704..166772350hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg3830647
hg1930647
hg1830647
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4973n100
Supporting Variantsnssv3612551
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)nsv1012124
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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