A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17690362



Internal ID114028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:101507001..101507067hg38UCSC Ensembl
chr12:101900779..101900845hg19UCSC Ensembl
Cytoband12q23.2
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5501477
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17690362
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.004215


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