A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5846192



Internal ID22621127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:19877938..19885801hg38UCSC Ensembl
chr7:19917561..19925424hg19UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg387864
hg197864
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1850n209
Supporting Variantsnssv17504708
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5846192
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