A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17077657



Internal ID21449954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:122695524..122695524hg38UCSC Ensembl
chr12:123180071..123180071hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg38450
hg19450
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5651949
Supporting Variants
SamplesHG01114
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17077657
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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