A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6066471



Internal ID21975704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:88502826..88502826hg38UCSC Ensembl
chr6:89212545..89212545hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg38312
hg19312
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17573301
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6066471
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