A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17472980



Internal ID22530872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:62106436..62116953hg38UCSC Ensembl
chr15:62398635..62409152hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg3810518
hg1910518
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5851626
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17472980
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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