A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063832



Internal ID18806363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42743361..42858488hg38UCSC Ensembl
Innerchr19:43247513..43362640hg19UCSC Ensembl
Innerchr19:47939353..48054480hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38115128
hg19115128
hg18115128
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3551n100
Supporting Variantsnssv3722796, nssv3722795, nssv3722797, nssv3568685, nssv3722794, nssv3568687, nssv3568686
Samples
Known GenesLOC100289650, PSG10P, PSG8
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1063832
Frequency
Sample Size29084
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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