A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579816



Internal ID16367225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:43158934..43335936hg38UCSC Ensembl
Innerchr19:43663086..43840088hg19UCSC Ensembl
Innerchr19:48354926..48531928hg18UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg38177003
hg19177003
hg18177003
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6497n54
Supporting Variantsnssv899859, nssv899863, nssv1151034, nssv899862, nssv899861, nssv899860
SamplesHGDP00057
Known GenesLOC284344, PSG4, PSG5, PSG9
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579816
Frequency
Sample Size17421
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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