A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5877096



Internal ID22652059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:88832767..89196074hg38UCSC Ensembl
chr2:89132280..89495562hg19UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38363308
hg19363283
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1156n209
Supporting Variantsnssv17406635
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5877096
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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