A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5510648



Internal ID287259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:77900015..77926344hg38UCSC Ensembl
chr14:78366358..78392687hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3826330
hg1926330
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17699400
Samples
Known GenesADCK1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5510648
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