A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5883336



Internal ID22658315
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:88861259..89234184hg38UCSC Ensembl
chr2:89160771..89533665hg19UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38372926
hg19372895
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1156n209
Supporting Variantsnssv17406636
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5883336
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