A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3644406



Internal ID6684473
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:42735427..42761031hg38UCSC Ensembl
Innerchr19:42735927..42760531hg38UCSC Ensembl
Outerchr19:42734427..42762031hg38UCSC Ensembl
chr19:43239579..43265183hg19UCSC Ensembl
Innerchr19:43240079..43264683hg19UCSC Ensembl
Outerchr19:43238579..43266183hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3825605
hg1925605
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16056321, essv16056323, essv16056324, essv16056322, essv16056325
SamplesHG01359, HG04185, HG01323, HG02970, HG01872
Known GenesPSG3, PSG8
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3644406
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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