A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5479579



Internal ID257098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:99986564..99987124hg38UCSC Ensembl
chr10:101746321..101746881hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg38561
hg19561
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17038436
Samples
Known GenesDNMBP
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5479579
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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