A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv891806



Internal ID15839076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:1475392..1540507hg38UCSC Ensembl
Innerchr19:1475391..1540506hg19UCSC Ensembl
Innerchr19:1426391..1491506hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3865116
hg1965116
hg1865116
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv578295
Supporting Variants
Samples
Known GenesADAMTSL5, C19orf25, PCSK4, PLK5, REEP6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv891806
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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