A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579895



Internal ID16020618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:47687915..47689925hg38UCSC Ensembl
Innerchr19:48191172..48193182hg19UCSC Ensembl
Innerchr19:52882984..52884994hg18UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg382011
hg192011
hg182011
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6507n54
Supporting Variantsnssv899981, nssv899982
Samples
Known GenesGLTSCR1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579895
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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