A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17700792



Internal ID124458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:56449327..56449364hg38UCSC Ensembl
chr15:56741525..56741562hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38320
hg19320
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5540576
Supporting Variants
Samples
Known GenesMNS1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17700792
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.055173


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