A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6068085



Internal ID21977318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:169153973..169153973hg38UCSC Ensembl
chr6:169554068..169554068hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38300
hg19300
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17572958
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6068085
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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