A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6063979



Internal ID21973212
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:142634461..142634461hg38UCSC Ensembl
chr6:142955598..142955598hg19UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg38299
hg19299
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17558509
Samples
Known GenesLOC153910
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6063979
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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