A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv899801



Internal ID16193757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42979717..43222743hg38UCSC Ensembl
Innerchr19:43483869..43726895hg19UCSC Ensembl
Innerchr19:48175709..48418735hg18UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg38243027
hg19243027
hg18243027
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv579768
Supporting Variants
Samples
Known GenesLOC284344, PSG11, PSG2, PSG4, PSG5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv899801
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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