A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5486571



Internal ID263932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:91168647..91168743hg38UCSC Ensembl
chr10:92928404..92928500hg19UCSC Ensembl
Cytoband10q23.32
Allele length
AssemblyAllele length
hg3897
hg1997
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17036873
Samples
Known GenesPCGF5
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5486571
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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