A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3643610



Internal ID7030369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:8180893..8187973hg38UCSC Ensembl
Innerchr19:8180945..8187922hg38UCSC Ensembl
Outerchr19:8180842..8188025hg38UCSC Ensembl
chr19:8245777..8252857hg19UCSC Ensembl
Innerchr19:8245829..8252806hg19UCSC Ensembl
Outerchr19:8245726..8252909hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg387081
hg197081
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15988763, essv15988764
SamplesHG02058, NA20586
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3643610
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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