A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5465617



Internal ID243476
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:96700901..96701035hg38UCSC Ensembl
chr5:96036605..96036739hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg38135
hg19135
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16971017
Samples
Known GenesCAST
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5465617
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer