A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17056482



Internal ID105474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:50372532..50372808hg38UCSC Ensembl
chr12:50766315..50766591hg19UCSC Ensembl
Cytoband12q13.12
Allele length
AssemblyAllele length
hg38277
hg19277
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5504072
Supporting Variants
Samples
Known GenesFAM186A
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17056482
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000469


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