A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15201540



Internal ID21340339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:96622859..96622859hg38UCSC Ensembl
chr5:95958563..95958563hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg38891
hg19891
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3946131
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15201540
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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