A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6016785



Internal ID21926128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:63179988..63180087hg38UCSC Ensembl
chr8:64092547..64092646hg19UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17586991
Samples
Known GenesYTHDF3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6016785
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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