A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18001292



Internal ID20568332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:50983028..50986546hg38UCSC Ensembl
chr12:51376811..51380329hg19UCSC Ensembl
Cytoband12q13.12
Allele length
AssemblyAllele length
hg383519
hg193519
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6456439
Supporting Variants
Samples
Known GenesSLC11A2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18001292
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00089


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