A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6072215



Internal ID21981448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:90037043..90037043hg38UCSC Ensembl
chr6:90746762..90746762hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg38315
hg19315
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17566586
Samples
Known GenesBACH2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6072215
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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