A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17077041



Internal ID21401326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:101478888..101478938hg38UCSC Ensembl
chr12:101872666..101872716hg19UCSC Ensembl
Cytoband12q23.2
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5600140
Supporting Variants
SamplesHG00096
Known GenesSPIC
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17077041
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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