A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18000023



Internal ID20567063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:26327850..26330008hg38UCSC Ensembl
chr12:26480783..26482941hg19UCSC Ensembl
Cytoband12p12.1
Allele length
AssemblyAllele length
hg382159
hg192159
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6460805
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18000023
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00013


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