A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6269n54



Internal ID20139693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:11930721..11934386hg38UCSC Ensembl
chr19:12041536..12045201hg19UCSC Ensembl
chr19:11902536..11906201hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg383666
hg193666
hg183666
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv578623, nsv578624
Samples
Known GenesZNF700
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv6269n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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