A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1062143



Internal ID19151362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:12405336..12429064hg38UCSC Ensembl
Innerchr19:12516150..12539878hg19UCSC Ensembl
Innerchr19:12377150..12400878hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3823729
hg1923729
hg1823729
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3433n100
Supporting Variantsnssv3723288, nssv3564713, nssv3564714
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)nsv1062143
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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