A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1003568



Internal ID18746099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:46760362..46808087hg38UCSC Ensembl
Innerchr3:46801852..46849577hg19UCSC Ensembl
Innerchr3:46776856..46824581hg18UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3847726
hg1947726
hg1847726
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4736n100
Supporting Variantsnssv3593778, nssv3593777
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)nsv1003568
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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