A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17471689



Internal ID22529581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:53328735..53329834hg38UCSC Ensembl
chr15:53620932..53622031hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg381100
hg191100
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5866446
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17471689
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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