A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17471908



Internal ID22529800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:45227334..45229133hg38UCSC Ensembl
chr15:45519532..45521331hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg381800
hg191800
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5851319
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17471908
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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