A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063937



Internal ID18806468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:6892758..7106712hg38UCSC Ensembl
Innerchr19:6892769..7106723hg19UCSC Ensembl
Innerchr19:6843769..7057723hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38213955
hg19213955
hg18213955
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3421n100
Supporting Variantsnssv3723272
Samples
Known GenesEMR1, EMR4P, FLJ25758, MBD3L2, MBD3L3, MBD3L4, MBD3L5, ZNF557
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1063937
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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