A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17076962



Internal ID21452746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:114084520..114084520hg38UCSC Ensembl
chr12:114522325..114522325hg19UCSC Ensembl
Cytoband12q24.21
Allele length
AssemblyAllele length
hg38627
hg19627
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5646863
Supporting Variants
SamplesHG01596
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17076962
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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