A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065141



Internal ID19154360
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42776064..43087618hg38UCSC Ensembl
Innerchr19:43280216..43591770hg19UCSC Ensembl
Innerchr19:47972056..48283610hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38311555
hg19311555
hg18311555
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3556n100
Supporting Variantsnssv3568901
Samples
Known GenesLOC100289650, PSG1, PSG10P, PSG11, PSG2, 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)nsv1065141
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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