A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3643741



Internal ID6683811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:14400728..14402421hg38UCSC Ensembl
Innerchr19:14400728..14402421hg38UCSC Ensembl
Outerchr19:14400452..14402708hg38UCSC Ensembl
chr19:14511540..14513233hg19UCSC Ensembl
Innerchr19:14511540..14513233hg19UCSC Ensembl
Outerchr19:14511264..14513520hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg381694
hg191694
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15997283, essv15997284
SamplesHG01072, HG01174
Known GenesCD97
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3643741
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