A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3634572



Internal ID7021375
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:55156009..55159308hg38UCSC Ensembl
Innerchr14:55156009..55159308hg38UCSC Ensembl
Outerchr14:55155767..55159619hg38UCSC Ensembl
chr14:55622727..55626026hg19UCSC Ensembl
Innerchr14:55622727..55626026hg19UCSC Ensembl
Outerchr14:55622485..55626337hg19UCSC Ensembl
Cytoband14q22.3
Allele length
AssemblyAllele length
hg383300
hg193300
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15019161
SamplesNA19716
Known GenesDLGAP5
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3634572
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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