A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5880772



Internal ID22655742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:19298715..19299916hg38UCSC Ensembl
chr1:19625209..19626410hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg381202
hg191202
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17353599
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5880772
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