A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3643812



Internal ID7030569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:17117789..17120015hg38UCSC Ensembl
Innerchr19:17117790..17120014hg38UCSC Ensembl
Outerchr19:17117788..17120016hg38UCSC Ensembl
chr19:17228599..17230825hg19UCSC Ensembl
Innerchr19:17228600..17230824hg19UCSC Ensembl
Outerchr19:17228598..17230826hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg382227
hg192227
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16002950
SamplesHG02620
Known GenesMYO9B
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3643812
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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