A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17080200



Internal ID21437283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:113841469..113841469hg38UCSC Ensembl
chr13:114544442..114544442hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5657026
Supporting Variants
SamplesHG00731
Known GenesGAS6, GAS6-AS1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17080200
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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