A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17096702



Internal ID21430460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:108215427..108215427hg38UCSC Ensembl
chr13:108867775..108867775hg19UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg3889
hg1989
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5652682
Supporting Variants
SamplesHG00731
Known GenesLIG4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17096702
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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