A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3644219



Internal ID7030975
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:34824923..34863571hg38UCSC Ensembl
Innerchr19:34824956..34863539hg38UCSC Ensembl
Outerchr19:34824891..34863604hg38UCSC Ensembl
chr19:35315827..35354475hg19UCSC Ensembl
Innerchr19:35315860..35354443hg19UCSC Ensembl
Outerchr19:35315795..35354508hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg3838649
hg1938649
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16044846, essv16044845, essv16044847
SamplesHG03121, HG03163, HG01049
Known GenesLOC400685
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3644219
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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