A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6015609



Internal ID21924952
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:141594623..141595040hg38UCSC Ensembl
chr5:140974190..140974607hg19UCSC Ensembl
Cytoband5q31.3
Allele length
AssemblyAllele length
hg38418
hg19418
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17551944
Samples
Known GenesDIAPH1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6015609
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