A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17471690



Internal ID22529582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:53426340..53427801hg38UCSC Ensembl
chr15:53718537..53719998hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg381462
hg191462
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5852233
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17471690
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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