A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3644643



Internal ID6684709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:50302681..50304376hg38UCSC Ensembl
Innerchr19:50302722..50304335hg38UCSC Ensembl
Outerchr19:50302640..50304417hg38UCSC Ensembl
chr19:50805938..50807633hg19UCSC Ensembl
Innerchr19:50805979..50807592hg19UCSC Ensembl
Outerchr19:50805897..50807674hg19UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg381696
hg191696
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16076059
SamplesHG00237
Known GenesMYH14
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3644643
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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