A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6074125



Internal ID21983358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:90233242..90233242hg38UCSC Ensembl
chr8:91245470..91245470hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg38448
hg19448
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17582304, nssv17596800
Samples
Known GenesLINC00534
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6074125
Frequency
Sample Size405
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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