A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5928323



Internal ID22703560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:96112149..96112813hg38UCSC Ensembl
chr15:96655378..96656042hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg38665
hg19665
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17383348
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5928323
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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