A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3643855



Internal ID7030612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:19701528..19702283hg38UCSC Ensembl
Innerchr19:19701556..19702255hg38UCSC Ensembl
Outerchr19:19701500..19702311hg38UCSC Ensembl
chr19:19812337..19813092hg19UCSC Ensembl
Innerchr19:19812365..19813064hg19UCSC Ensembl
Outerchr19:19812309..19813120hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg38756
hg19756
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16005743, essv16005742
SamplesHG02398, HG00978
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3643855
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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