A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5470757



Internal ID248505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:40314733..40315470hg38UCSC Ensembl
chr4:40316750..40317487hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg38738
hg19738
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16948118
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5470757
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