A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5464721



Internal ID242592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:75463863..75467174hg38UCSC Ensembl
chr5:74759688..74762999hg19UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg383312
hg193312
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16968370
Samples
Known GenesCOL4A3BP
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5464721
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