A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3644384



Internal ID7031139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:41502624..41524011hg38UCSC Ensembl
Innerchr19:41503124..41523511hg38UCSC Ensembl
Outerchr19:41501624..41525011hg38UCSC Ensembl
chr19:42008540..42030371hg19UCSC Ensembl
Innerchr19:42009040..42029871hg19UCSC Ensembl
Outerchr19:42007540..42031371hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3821388
hg1921832
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16056097, essv16056094, essv16056096, essv16056093, essv16056092, essv16056095
SamplesNA18988, NA19130, NA18874, HG00131, NA18984, NA19004
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3644384
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