A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6071699



Internal ID21980932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:167997484..167997484hg38UCSC Ensembl
chr6:168398164..168398164hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38541
hg19541
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17561156
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6071699
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer