A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17076497



Internal ID21506217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:102523914..102523914hg38UCSC Ensembl
chr12:102917692..102917692hg19UCSC Ensembl
Cytoband12q23.2
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5650770
Supporting Variants
SamplesNA19983
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17076497
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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