A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18000001



Internal ID20567041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:25936260..25939534hg38UCSC Ensembl
chr12:26089193..26092467hg19UCSC Ensembl
Cytoband12p12.1
Allele length
AssemblyAllele length
hg383275
hg193275
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6460743
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18000001
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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