A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6062689



Internal ID21971922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:13925069..13925069hg38UCSC Ensembl
chr6:13925300..13925300hg19UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg38182
hg19182
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17560363
Samples
Known GenesRNF182
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6062689
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