A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6097019



Internal ID22006252
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 StatusM
Merged Variants
Supporting Variantsnssv17620831
Samples
Known GenesTMUB2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6097019
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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