A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17996108



Internal ID20563148
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:106320531..106322521hg38UCSC Ensembl
chr12:106714309..106716299hg19UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg381991
hg191991
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6475118
Supporting Variants
Samples
Known GenesTCP11L2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17996108
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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