A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5484612



Internal ID262023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:37372121..37396292hg38UCSC Ensembl
chr10:37661049..37685220hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg3824172
hg1924172
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17031631
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5484612
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