A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17566889



Internal ID21758932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:30177256..30177307hg38UCSC Ensembl
chr8:30034772..30034823hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6014273
Supporting Variants
Samples
Known GenesDCTN6, MIR548O2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17566889
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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