A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17374628



Internal ID22600297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:89908403..89909371hg38UCSC Ensembl
chr15:90451635..90452603hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38969
hg19969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5944916
Supporting Variants
Samples
Known GenesC15orf38, C15orf38-AP3S2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17374628
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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