A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6002599



Internal ID21911942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:31149280..31149346hg38UCSC Ensembl
chr8:31006796..31006862hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17564228
Samples
Known GenesWRN
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6002599
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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