A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv899606



Internal ID16193562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42752863..42843934hg38UCSC Ensembl
Innerchr19:43257015..43348086hg19UCSC Ensembl
Innerchr19:47948855..48039926hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3891072
hg1991072
hg1891072
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv579634
Supporting Variants
Samples
Known GenesLOC100289650, PSG10P, PSG8
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv899606
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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