A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5883842



Internal ID22658824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:46240191..46242953hg38UCSC Ensembl
chr1:46705863..46708625hg19UCSC Ensembl
Cytoband1p34.1
Allele length
AssemblyAllele length
hg382763
hg192763
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17382192
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5883842
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