A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5962170



Internal ID22737106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:91168263..91168263hg38UCSC Ensembl
chr5:90464080..90464080hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg38186
hg19186
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17426401
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5962170
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