A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5458150



Internal ID236179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:44401675..44402361hg38UCSC Ensembl
chr5:44401777..44402463hg19UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg38687
hg19687
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16965414
Samples
Known GenesFGF10-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5458150
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