A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3643740



Internal ID7030498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:14366169..14368823hg38UCSC Ensembl
Innerchr19:14366174..14368818hg38UCSC Ensembl
Outerchr19:14366164..14368828hg38UCSC Ensembl
chr19:14476981..14479635hg19UCSC Ensembl
Innerchr19:14476986..14479630hg19UCSC Ensembl
Outerchr19:14476976..14479640hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg382655
hg192655
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15997262, essv15997257, essv15997258, essv15997264, essv15997279, essv15997270, essv15997275, essv15997281, essv15997267, essv15997269, essv15997277, essv15997276, essv15997282, essv15997280, essv15997272, essv15997265, essv15997268, essv15997271, essv15997273, essv15997259, essv15997274, essv15997260, essv15997278, essv15997261, essv15997263, essv15997266
SamplesHG03773, HG04060, NA21100, HG03015, HG02600, HG03009, HG04042, HG04183, HG03788, HG03696, HG04020, HG02780, NA21106, NA20892, NA21119, HG03786, NA20876, NA21124, HG04054, HG03971, NA21144, HG03779, NA21125, HG03642, HG03849, NA21104
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3643740
Frequency
Sample Size2504
Observed Gain0
Observed Loss26
Observed Complex0
Frequencyn/a


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