A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18193268



Internal ID20760308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:110388929..110389808hg38UCSC Ensembl
chr12:110826734..110827613hg19UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg38880
hg19880
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6477966
Supporting Variants
Samples
Known GenesANAPC7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18193268
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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