A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5487192



Internal ID264536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:28598348..28598470hg38UCSC Ensembl
chr10:28887277..28887399hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg38123
hg19123
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17033421
Samples
Known GenesWAC
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5487192
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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