A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17606122



Internal ID21798169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:94613050..94613050hg38UCSC Ensembl
chr12:95006826..95006826hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6083903
Supporting Variants
Samples
Known GenesTMCC3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17606122
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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