A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17077887



Internal ID21447455
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:119693031..119693031hg38UCSC Ensembl
chr12:120130836..120130836hg19UCSC Ensembl
Cytoband12q24.23
Allele length
AssemblyAllele length
hg38365
hg19365
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5655628
Supporting Variants
SamplesHG00732
Known GenesCIT
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17077887
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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