A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17996267



Internal ID20563307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:109591582..109601249hg38UCSC Ensembl
chr12:110029387..110039054hg19UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg389668
hg199668
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6488556
Supporting Variants
Samples
Known GenesMVK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17996267
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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