A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6013519



Internal ID21922862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:148457904..148457982hg38UCSC Ensembl
chr5:147837467..147837545hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17561349
Samples
Known GenesHTR4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6013519
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