A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17077649



Internal ID21472680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:122390282..122390282hg38UCSC Ensembl
chr12:122874829..122874829hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5649936
Supporting Variants
SamplesHG03371
Known GenesCLIP1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17077649
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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