A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6058049



Internal ID21967282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:169554165..169554165hg38UCSC Ensembl
chr1:169523403..169523403hg19UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg3894
hg1994
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17536404
Samples
Known GenesF5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6058049
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