A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6215n54



Internal ID20139639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:2014038..2015023hg38UCSC Ensembl
chr19:2014037..2015022hg19UCSC Ensembl
chr19:1965037..1966022hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38986
hg19986
hg18986
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv578375, nsv578372, nsv578373, nsv578368
Samples
Known GenesBTBD2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv6215n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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