A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17079258



Internal ID21459208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:27062412..27062412hg38UCSC Ensembl
chr12:27215345..27215345hg19UCSC Ensembl
Cytoband12p11.23
Allele length
AssemblyAllele length
hg38131
hg19131
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5651157
Supporting Variants
SamplesHG02818
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17079258
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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