A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17085945



Internal ID21491027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:92496077..92496077hg38UCSC Ensembl
chr12:92889853..92889853hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg38323
hg19323
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5647279
Supporting Variants
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17085945
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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