A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6048881



Internal ID21958115
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:53086992..53086992hg38UCSC Ensembl
chr1:53552664..53552664hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17517758
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6048881
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