A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1056871



Internal ID18799402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42720398..42857538hg38UCSC Ensembl
Innerchr19:43224550..43361690hg19UCSC Ensembl
Innerchr19:47916390..48053530hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38137141
hg19137141
hg18137141
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3551n100
Supporting Variantsnssv3722785
Samples
Known GenesLOC100289650, PSG10P, PSG3, PSG8
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1056871
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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