A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5865656



Internal ID22640591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:82653953..82655281hg38UCSC Ensembl
chr13:83228088..83229416hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg381329
hg191329
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17456286, nssv17462205
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5865656
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