A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17096020



Internal ID21446739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:36142665..36142665hg38UCSC Ensembl
chr13:36716802..36716802hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg38295
hg19295
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5653455
Supporting Variants
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17096020
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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