A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5952469



Internal ID22727782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:151140577..151140577hg38UCSC Ensembl
chr5:150520138..150520138hg19UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17428220
Samples
Known GenesANXA6
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5952469
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