A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15186887



Internal ID21325717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:35527213..35527213hg38UCSC Ensembl
chr19:36018115..36018115hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg38216
hg19216
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3943744
Supporting Variants
SamplesHG002
Known GenesSBSN
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15186887
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer