A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5485471



Internal ID262860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:44529156..44531462hg38UCSC Ensembl
chr10:45024604..45026910hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg382307
hg192307
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17034968
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5485471
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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