A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18000137



Internal ID20567177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:28170520..28170969hg38UCSC Ensembl
chr12:28323453..28323902hg19UCSC Ensembl
Cytoband12p11.22
Allele length
AssemblyAllele length
hg38450
hg19450
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6458953
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18000137
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00066


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