A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17620063



Internal ID21812110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:57450268..57450268hg38UCSC Ensembl
chr17:55527629..55527629hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38109
hg19109
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6084914
Supporting Variants
Samples
Known GenesMSI2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17620063
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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