A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6016644



Internal ID21925987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:172049964..172050874hg38UCSC Ensembl
chr5:171476968..171477878hg19UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg38911
hg19911
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17557771
Samples
Known GenesSTK10
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6016644
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