A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5495970



Internal ID273062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:111144258..111182043hg38UCSC Ensembl
chr10:112904016..112941801hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg3837786
hg1937786
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17041102
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5495970
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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