A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6049568



Internal ID21958801
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:69066548..69066548hg38UCSC Ensembl
chr1:69532231..69532231hg19UCSC Ensembl
Cytoband1p31.2
Allele length
AssemblyAllele length
hg38309
hg19309
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17529630
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6049568
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