A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17997658



Internal ID20564698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:15929604..15937208hg38UCSC Ensembl
chr12:16082538..16090142hg19UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg387605
hg197605
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6467861
Supporting Variants
Samples
Known GenesDERA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17997658
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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