A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17077162



Internal ID21457845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:110955832..110955832hg38UCSC Ensembl
chr12:111393636..111393636hg19UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg38470
hg19470
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5645398
Supporting Variants
SamplesHG02587
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17077162
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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