A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17557368



Internal ID21881723
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:81987677..82058493hg38UCSC Ensembl
chr5:81283496..81354312hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg3870817
hg1970817
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6016735
Supporting Variants
Samples
Known GenesATG10
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17557368
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