A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6079886



Internal ID21989119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:91562940..91562940hg38UCSC Ensembl
chr6:92272658..92272658hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg381155
hg191155
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17576174
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6079886
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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