A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6210n54



Internal ID20139634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:1862991..1864757hg38UCSC Ensembl
chr19:1862990..1864756hg19UCSC Ensembl
chr19:1813990..1815756hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg381767
hg191767
hg181767
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv578343, nsv578342
Samples
Known GenesKLF16
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv6210n54
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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