A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15193011



Internal ID21331896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:94597249..94597249hg38UCSC Ensembl
chr13:95249503..95249503hg19UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg38145
hg19145
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3939989
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15193011
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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