A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv899895



Internal ID15847165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:43290434..43366735hg38UCSC Ensembl
Innerchr19:43794586..43870887hg19UCSC Ensembl
Innerchr19:48486426..48562727hg18UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg3876302
hg1976302
hg1876302
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv579843
Supporting Variants
Samples
Known GenesCD177, PRG1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv899895
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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