A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5490242



Internal ID267503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:59598000..59619000hg38UCSC Ensembl
chr10:61357758..61378758hg19UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg3821001
hg1921001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17036277
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5490242
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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