A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5483937



Internal ID261363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:60606978..60614869hg38UCSC Ensembl
chr10:62366736..62374627hg19UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg387892
hg197892
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17035914
Samples
Known GenesANK3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5483937
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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