A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3643494



Internal ID6683566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:4275790..4289414hg38UCSC Ensembl
Innerchr19:4276290..4288914hg38UCSC Ensembl
Outerchr19:4274790..4290414hg38UCSC Ensembl
chr19:4275787..4289411hg19UCSC Ensembl
Innerchr19:4276287..4288911hg19UCSC Ensembl
Outerchr19:4274787..4290411hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3813625
hg1913625
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15980399
SamplesNA11920
Known GenesSHD
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3643494
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