A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3644341



Internal ID6684409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:40085158..40087032hg38UCSC Ensembl
Innerchr19:40085162..40087029hg38UCSC Ensembl
Outerchr19:40085155..40087036hg38UCSC Ensembl
chr19:40591065..40592939hg19UCSC Ensembl
Innerchr19:40591069..40592936hg19UCSC Ensembl
Outerchr19:40591062..40592943hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg381875
hg191875
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16054650
SamplesHG04219
Known GenesZNF780A
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3644341
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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