A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5481636



Internal ID259109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:70020923..70049310hg38UCSC Ensembl
chr10:71780679..71809066hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg3828388
hg1928388
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17035182
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5481636
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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