A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3635587



Internal ID7022386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:103312994..103317885hg38UCSC Ensembl
Innerchr14:103313044..103317835hg38UCSC Ensembl
Outerchr14:103312932..103317947hg38UCSC Ensembl
chr14:103779331..103784222hg19UCSC Ensembl
Innerchr14:103779381..103784172hg19UCSC Ensembl
Outerchr14:103779269..103784284hg19UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg384892
hg194892
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15114315, essv15114310, essv15114312, essv15114314, essv15114313, essv15114311
SamplesHG02645, HG03061, NA19152, NA18933, HG03565, HG02107
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3635587
Frequency
Sample Size2504
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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