A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6506n54



Internal ID18998682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:47686937..47689925hg38UCSC Ensembl
chr19:48190194..48193182hg19UCSC Ensembl
chr19:52882006..52884994hg18UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg382989
hg192989
hg182989
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv579893, nsv579892, nsv579891, nsv579890
Samples
Known GenesGLTSCR1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv6506n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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