A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15194305



Internal ID21333201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:51070888..51070888hg38UCSC Ensembl
chr13:51645024..51645024hg19UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg38130
hg19130
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3928889
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15194305
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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