A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6010535



Internal ID21919878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:100316139..100316242hg38UCSC Ensembl
chr8:101328367..101328470hg19UCSC Ensembl
Cytoband8q22.2
Allele length
AssemblyAllele length
hg38104
hg19104
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17592509
Samples
Known GenesRNF19A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6010535
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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