A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3643751



Internal ID6683821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:14797644..14810922hg38UCSC Ensembl
Innerchr19:14797663..14810904hg38UCSC Ensembl
Outerchr19:14797626..14810941hg38UCSC Ensembl
chr19:14908456..14921734hg19UCSC Ensembl
Innerchr19:14908475..14921716hg19UCSC Ensembl
Outerchr19:14908438..14921753hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3813279
hg1913279
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15997476
SamplesNA20786
Known GenesOR7C1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3643751
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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