A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16268990



Internal ID20478208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:42165833..42167673hg38UCSC Ensembl
chr5:42165935..42167775hg19UCSC Ensembl
Cytoband5p13.1
Allele length
AssemblyAllele length
hg381841
hg191841
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4746665
Supporting Variants
Samples
Known GenesLOC101926960
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16268990
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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