A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5977231



Internal ID22752166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:20882127..20882127hg38UCSC Ensembl
chr13:21456266..21456266hg19UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg38158
hg19158
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17373732
Samples
Known GenesXPO4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5977231
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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