A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv899619



Internal ID16193575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42767839..42864809hg38UCSC Ensembl
Innerchr19:43271991..43368961hg19UCSC Ensembl
Innerchr19:47963831..48060801hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3896971
hg1996971
hg1896971
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv579643
Supporting Variants
Samples
Known GenesLOC100289650, PSG10P
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv899619
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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