A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3633835



Internal ID7020641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:25665855..25667420hg38UCSC Ensembl
Innerchr14:25665861..25667415hg38UCSC Ensembl
Outerchr14:25665850..25667426hg38UCSC Ensembl
chr14:26135061..26136626hg19UCSC Ensembl
Innerchr14:26135067..26136621hg19UCSC Ensembl
Outerchr14:26135056..26136632hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg381566
hg191566
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14945259, essv14945261, essv14945262, essv14945258, essv14945260
SamplesNA19098, HG03394, NA19043, NA19035, HG03469
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3633835
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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