A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17473602



Internal ID22531495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:72418547..72425196hg38UCSC Ensembl
chr15:72710888..72717537hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg386650
hg196650
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5851137
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17473602
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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