A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5484930



Internal ID262328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:49011906..49038632hg38UCSC Ensembl
chr10:50219951..50246677hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg3826727
hg1926727
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17036032
Samples
Known GenesVSTM4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5484930
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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