A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15193454



Internal ID21332344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:26242117..26242117hg38UCSC Ensembl
chr13:26816254..26816254hg19UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg38318
hg19318
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3954455
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15193454
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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