A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17474881



Internal ID22532776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:89859739..89864388hg38UCSC Ensembl
chr15:90402971..90407620hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg384650
hg194650
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5885468
Supporting Variants
Samples
Known GenesAP3S2, C15orf38-AP3S2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17474881
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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