A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5480969



Internal ID258465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:62665900..62671133hg38UCSC Ensembl
chr10:64425660..64430893hg19UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg385234
hg195234
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17033999
Samples
Known GenesZNF365
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5480969
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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