A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5488101



Internal ID265421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:13395145..13395445hg38UCSC Ensembl
chr10:13437145..13437445hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38301
hg19301
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17030269
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5488101
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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