A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17077219



Internal ID21505341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:115599930..115599930hg38UCSC Ensembl
chr12:116037735..116037735hg19UCSC Ensembl
Cytoband12q24.21
Allele length
AssemblyAllele length
hg38132
hg19132
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5659523
Supporting Variants
SamplesNA19650
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17077219
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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