A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17474880



Internal ID22532775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:89856000..89867711hg38UCSC Ensembl
chr15:90399232..90410943hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3811712
hg1911712
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5868458
Supporting Variants
Samples
Known GenesAP3S2, C15orf38-AP3S2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17474880
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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