A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15176730



Internal ID21315526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:46389403..46389459hg38UCSC Ensembl
chr19:46892660..46892716hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3950928
Supporting Variants
SamplesHG002
Known GenesPPP5C
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15176730
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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