A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15192974



Internal ID21331862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:78659312..78659312hg38UCSC Ensembl
chr13:79233447..79233447hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg38104
hg19104
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3948089
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15192974
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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