A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15193576



Internal ID21332467
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 StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3938043
Supporting Variants
SamplesHG002
Known GenesLIG4
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15193576
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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