A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3643673



Internal ID6683744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:11523953..11528541hg38UCSC Ensembl
Innerchr19:11524006..11528488hg38UCSC Ensembl
Outerchr19:11523900..11528594hg38UCSC Ensembl
chr19:11634768..11639356hg19UCSC Ensembl
Innerchr19:11634821..11639303hg19UCSC Ensembl
Outerchr19:11634715..11639409hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg384589
hg194589
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15990795
SamplesHG02006
Known GenesECSIT
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3643673
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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