A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3644373



Internal ID7031129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:41142943..41145574hg38UCSC Ensembl
Innerchr19:41143093..41145424hg38UCSC Ensembl
Outerchr19:41142793..41145724hg38UCSC Ensembl
chr19:41648848..41651479hg19UCSC Ensembl
Innerchr19:41648998..41651329hg19UCSC Ensembl
Outerchr19:41648698..41651629hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg382632
hg192632
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16055673
SamplesNA20901
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3644373
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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