A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5955091



Internal ID22730314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:11969987..11969987hg38UCSC Ensembl
chr6:11970220..11970220hg19UCSC Ensembl
Cytoband6p24.1
Allele length
AssemblyAllele length
hg38245
hg19245
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17411674
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5955091
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