A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5871956



Internal ID22646894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:38230607..38243302hg38UCSC Ensembl
chr19:38721247..38733942hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3812696
hg1912696
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17475352
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5871956
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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