A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv899868



Internal ID16193824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:43158934..43349353hg38UCSC Ensembl
Innerchr19:43663086..43853505hg19UCSC Ensembl
Innerchr19:48354926..48545345hg18UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg38190420
hg19190420
hg18190420
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv579819
Supporting Variants
Samples
Known GenesLOC284344, PRG1, PSG4, PSG5, PSG9
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv899868
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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