A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6010336



Internal ID21919679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:53136642..53136703hg38UCSC Ensembl
chr8:54049202..54049263hg19UCSC Ensembl
Cytoband8q11.23
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17592588
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6010336
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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