A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15194401



Internal ID21333305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:111621615..111621615hg38UCSC Ensembl
chr13:112273962..112273962hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38663
hg19663
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3937041
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15194401
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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