A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5876305



Internal ID22651265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:24150845..24153001hg38UCSC Ensembl
chr1:24477335..24479491hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg382157
hg192157
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17365611
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5876305
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