A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1006720



Internal ID19095938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:65202778..65224628hg38UCSC Ensembl
Innerchr3:65188453..65210303hg19UCSC Ensembl
Innerchr3:65163493..65185343hg18UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3821851
hg1921851
hg1821851
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4761n100
Supporting Variantsnssv3594750
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)nsv1006720
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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