A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6010827



Internal ID21920170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:112955030..112955285hg38UCSC Ensembl
chr5:112290727..112290982hg19UCSC Ensembl
Cytoband5q22.2
Allele length
AssemblyAllele length
hg38256
hg19256
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17542630
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6010827
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer