A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17548529



Internal ID21872884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:81981418..81987553hg38UCSC Ensembl
chr5:81277237..81283372hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg386136
hg196136
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6006992
Supporting Variants
Samples
Known GenesATG10
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17548529
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