A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17620831



Internal ID21812878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:44191362..44191362hg38UCSC Ensembl
chr17:42268730..42268730hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg38295
hg19295
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6097019
Supporting Variants
Samples
Known GenesTMUB2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17620831
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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