A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16002708



Internal ID3088416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:15998820..16006529hg38UCSC Ensembl
Innerchr19:15998832..16006517hg38UCSC Ensembl
Outerchr19:15998808..16006541hg38UCSC Ensembl
chr19:16109630..16117339hg19UCSC Ensembl
Innerchr19:16109642..16117327hg19UCSC Ensembl
Outerchr19:16109618..16117351hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg387710
hg197710
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3643787
Supporting Variants
SamplesHG02715
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv16002708
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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