A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5876267



Internal ID22651227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:153017240..153017361hg38UCSC Ensembl
chr1:152989716..152989837hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg38122
hg19122
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17350183
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5876267
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