A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6100053



Internal ID22009286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:63381936..63381936hg38UCSC Ensembl
chr17:61459297..61459297hg19UCSC Ensembl
Cytoband17q23.3
Allele length
AssemblyAllele length
hg38588
hg19588
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17636534
Samples
Known GenesTANC2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6100053
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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