A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18180965



Internal ID20748005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:112514532..112527388hg38UCSC Ensembl
chr12:112952336..112965192hg19UCSC Ensembl
Cytoband12q24.13
Allele length
AssemblyAllele length
hg3812857
hg1912857
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6489827
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18180965
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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