A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17372350



Internal ID22598019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:96099711..96100416hg38UCSC Ensembl
chr15:96642940..96643645hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg38706
hg19706
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5940963
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17372350
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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