A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17689804



Internal ID113470
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:86341629..86382110hg38UCSC Ensembl
chr12:86735407..86775888hg19UCSC Ensembl
Cytoband12q21.32
Allele length
AssemblyAllele length
hg3840482
hg1940482
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5501454
Supporting Variants
Samples
Known GenesMGAT4C
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17689804
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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