A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17468361



Internal ID22526250
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:2964666..2972065hg38UCSC Ensembl
chr12:3073832..3081231hg19UCSC Ensembl
Cytoband12p13.33
Allele length
AssemblyAllele length
hg387400
hg197400
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5850843
Supporting Variants
Samples
Known GenesTEAD4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17468361
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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