A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5485157



Internal ID262554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:89633678..89638667hg38UCSC Ensembl
chr10:91393435..91398424hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg384990
hg194990
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17036438
Samples
Known GenesPANK1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5485157
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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