A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6078062



Internal ID21987295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:170030080..170030080hg38UCSC Ensembl
chr6:170345304..170345304hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38277
hg19277
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17575261
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6078062
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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