A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17616217



Internal ID21808264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:110625645..110625713hg38UCSC Ensembl
chr12:111063450..111063518hg19UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6024118
Supporting Variants
Samples
Known GenesTCTN1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17616217
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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