A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5887125



Internal ID22662117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:88860917..89213421hg38UCSC Ensembl
chr2:89160429..89512906hg19UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38352505
hg19352478
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1156n209
Supporting Variantsnssv17405536
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5887125
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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