A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17997779



Internal ID20564819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:121670609..121671130hg38UCSC Ensembl
chr12:122108515..122109036hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg38522
hg19522
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6486571
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17997779
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00012


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