A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3643858



Internal ID6683927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:19816649..19818108hg38UCSC Ensembl
Innerchr19:19816649..19818108hg38UCSC Ensembl
Outerchr19:19816322..19818329hg38UCSC Ensembl
chr19:19927458..19928917hg19UCSC Ensembl
Innerchr19:19927458..19928917hg19UCSC Ensembl
Outerchr19:19927131..19929138hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg381460
hg191460
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16006928, essv16006929
SamplesHG02725, HG02727
Known GenesZNF506
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3643858
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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