A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15997618



Internal ID5983304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:14922710..14932035hg38UCSC Ensembl
Innerchr19:14923210..14931535hg38UCSC Ensembl
Outerchr19:14921710..14933035hg38UCSC Ensembl
chr19:15033522..15042847hg19UCSC Ensembl
Innerchr19:15034022..15042347hg19UCSC Ensembl
Outerchr19:15032522..15043847hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg389326
hg199326
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3643757
Supporting Variants
SamplesNA19390
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15997618
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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