A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065531



Internal ID19154750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42790226..43056212hg38UCSC Ensembl
Innerchr19:43294378..43560364hg19UCSC Ensembl
Innerchr19:47986218..48252204hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38265987
hg19265987
hg18265987
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3556n100
Supporting Variantsnssv3569497
Samples
Known GenesLOC100289650, PSG1, PSG10P, PSG11, PSG6, PSG7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1065531
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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