A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5499487



Internal ID276459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:125409695..125422395hg38UCSC Ensembl
chr10:127098264..127110964hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3812701
hg1912701
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17038923
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5499487
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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