A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3644232



Internal ID6684300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:35253087..35263050hg38UCSC Ensembl
Innerchr19:35253150..35262988hg38UCSC Ensembl
Outerchr19:35253025..35263113hg38UCSC Ensembl
chr19:35743990..35753953hg19UCSC Ensembl
Innerchr19:35744053..35753891hg19UCSC Ensembl
Outerchr19:35743928..35754016hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg389964
hg199964
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16045673, essv16045672
SamplesNA19917, HG00690
Known GenesLSR
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3644232
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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