A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17996244



Internal ID20563284
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:109046875..109051371hg38UCSC Ensembl
chr12:109484680..109489176hg19UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg384497
hg194497
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6487231
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17996244
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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