A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5876582



Internal ID22651543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:31365029..31366028hg38UCSC Ensembl
chr19:31855935..31856934hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17474679
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5876582
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