A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6005944



Internal ID21915287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:68160004..68168660hg38UCSC Ensembl
chr8:69072239..69080895hg19UCSC Ensembl
Cytoband8q13.2
Allele length
AssemblyAllele length
hg388657
hg198657
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17593888
Samples
Known GenesPREX2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6005944
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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