A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5492690



Internal ID269895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:16004050..16004316hg38UCSC Ensembl
chr10:16046049..16046315hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38267
hg19267
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17030357
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5492690
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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