A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17472344



Internal ID22530236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:82927683..82929642hg38UCSC Ensembl
chr15:83596435..83598394hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg381960
hg191960
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5859667
Supporting Variants
Samples
Known GenesHOMER2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17472344
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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