A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5964055



Internal ID22738990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:69680944..69680944hg38UCSC Ensembl
chr10:71440700..71440700hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg38300
hg19300
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17350027
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5964055
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