A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18183733



Internal ID20750773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:111613462..111645347hg38UCSC Ensembl
chr12:112051266..112083151hg19UCSC Ensembl
Cytoband12q24.12
Allele length
AssemblyAllele length
hg3831886
hg1931886
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6479181
Supporting Variants
Samples
Known GenesBRAP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18183733
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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