A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17689287



Internal ID112953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:76721559..76724452hg38UCSC Ensembl
chr12:77115339..77118232hg19UCSC Ensembl
Cytoband12q21.2
Allele length
AssemblyAllele length
hg382894
hg192894
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5508919
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17689287
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.006088


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