A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6002091



Internal ID21911434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:51533463..51535745hg38UCSC Ensembl
chr8:52446023..52448305hg19UCSC Ensembl
Cytoband8q11.22
Allele length
AssemblyAllele length
hg382283
hg192283
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17592476
Samples
Known GenesPXDNL
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6002091
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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