A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579636



Internal ID16020359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42752863..42886210hg38UCSC Ensembl
Innerchr19:43257015..43390362hg19UCSC Ensembl
Innerchr19:47948855..48082202hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38133348
hg19133348
hg18133348
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6462n54
Supporting Variantsnssv899608
Samples
Known GenesLOC100289650, PSG1, PSG10P, PSG8
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579636
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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