A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17087482



Internal ID21453552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:112916193..112916193hg38UCSC Ensembl
chr13:113570507..113570507hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg383040
hg193040
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5648842
Supporting Variants
SamplesHG02011
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17087482
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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