A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5915027



Internal ID22690245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:42602801..42602850hg38UCSC Ensembl
chr10:43098249..43098298hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17357227
Samples
Known GenesZNF33B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5915027
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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