A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055516



Internal ID19144735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42760186..43044850hg38UCSC Ensembl
Innerchr19:43264338..43549002hg19UCSC Ensembl
Innerchr19:47956178..48240842hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38284665
hg19284665
hg18284665
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3556n100
Supporting Variantsnssv3568860
Samples
Known GenesLOC100289650, PSG1, PSG10P, PSG11, PSG6, PSG7, PSG8
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1055516
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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