A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6007715



Internal ID21917058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:165254657..165254725hg38UCSC Ensembl
chr5:164681663..164681731hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17560841
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6007715
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