A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5475657



Internal ID253293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:72640924..72662249hg38UCSC Ensembl
chr10:74400682..74422007hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg3821326
hg1921326
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17037550
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5475657
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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