A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17606679



Internal ID21798726
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:56460009..56460009hg38UCSC Ensembl
chr15:56752207..56752207hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6090372
Supporting Variants
Samples
Known GenesMNS1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17606679
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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