A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1002879



Internal ID19092096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:105426670..105532790hg38UCSC Ensembl
Innerchr1:105969292..106075412hg19UCSC Ensembl
Innerchr1:105770815..105876935hg18UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg38106121
hg19106121
hg18106121
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv236n100
Supporting Variantsnssv3484452, nssv3499754, nssv3501268
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)nsv1002879
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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