A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17076926



Internal ID21488498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:105547457..105550687hg38UCSC Ensembl
chr12:105941235..105944465hg19UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg383231
hg193231
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5588210
Supporting Variants
SamplesNA18939
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17076926
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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