A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3643n54



Internal ID22771538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:37754070..37793557hg38UCSC Ensembl
chr14:38223275..38262762hg19UCSC Ensembl
chr14:37293026..37332513hg18UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3839488
hg1939488
hg1839488
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv564384, nsv564383
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3643n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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