A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17084722



Internal ID21486256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:112282119..112282119hg38UCSC Ensembl
chr13:112936433..112936433hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38510
hg19510
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5650128
Supporting Variants
SamplesNA12878
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17084722
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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