A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6174n54



Internal ID18998350
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:579450..593319hg38UCSC Ensembl
chr19:579450..593319hg19UCSC Ensembl
chr19:530450..544319hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3813870
hg1913870
hg1813870
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv578162, nsv578155
Samples
Known GenesBSG, HCN2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv6174n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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