A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6318n54



Internal ID20139742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:20606450..20866398hg38UCSC Ensembl
chr19:20789256..21049204hg19UCSC Ensembl
chr19:20581096..20841044hg18UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38259949
hg19259949
hg18259949
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv578921, nsv578926, nsv578936, nsv578918, nsv578917, nsv578935
Samples1780862577_A
Known GenesZNF626
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv6318n54
Frequency
Sample Size17421
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer