A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5879235



Internal ID22654204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:35314370..35318143hg38UCSC Ensembl
chr1:35779971..35783744hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg383774
hg193774
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17379301
Samples
Known GenesZMYM4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5879235
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