A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3950047



Internal ID21370116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:3173290..3175554hg38UCSC Ensembl
chr19:3173288..3175552hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg382265
hg192265
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv22n167
Supporting Variantsnssv15177516
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3950047
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