A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6077567



Internal ID21986800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:158233859..158233859hg38UCSC Ensembl
chr6:158654891..158654891hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg38294
hg19294
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17558025
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6077567
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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