A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17079094



Internal ID21502885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:14843251..14843251hg38UCSC Ensembl
chr12:14996185..14996185hg19UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg38523
hg19523
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5654341
Supporting Variants
SamplesNA19239
Known GenesART4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17079094
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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