A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16051232



Internal ID5662433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:37365597..37368917hg38UCSC Ensembl
Innerchr19:37365626..37368888hg38UCSC Ensembl
Outerchr19:37365568..37368946hg38UCSC Ensembl
chr19:37856499..37859819hg19UCSC Ensembl
Innerchr19:37856528..37859790hg19UCSC Ensembl
Outerchr19:37856470..37859848hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg383321
hg193321
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3644286
Supporting Variants
SamplesNA19072
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv16051232
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