A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579892



Internal ID16020615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:47687016..47689867hg38UCSC Ensembl
Innerchr19:48190273..48193124hg19UCSC Ensembl
Innerchr19:52882085..52884936hg18UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg382852
hg192852
hg182852
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6506n54
Supporting Variantsnssv899977, nssv899978
Samples
Known GenesGLTSCR1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579892
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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