A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17472878



Internal ID22530770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:53912478..53921652hg38UCSC Ensembl
chr15:54204675..54213849hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg389175
hg199175
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5860701
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17472878
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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