A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5540576



Internal ID315321
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 StatusM
Merged Variants
Supporting Variantsnssv17700792
Samples
Known GenesMNS1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5540576
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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