A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6008756



Internal ID21918099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:141658448..142255360hg38UCSC Ensembl
chr8:142668548..143336721hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg38596913
hg19668174
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17580892
Samples
Known GenesLINC00051, MIR4472-1, TSNARE1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6008756
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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