A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17684228



Internal ID107894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:95101160..95102079hg38UCSC Ensembl
chr12:95494936..95495855hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg38920
hg19920
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5495857
Supporting Variants
Samples
Known GenesFGD6
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17684228
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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