A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5896102



Internal ID22671191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:2862496..2863086hg38UCSC Ensembl
chr5:2862610..2863200hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg38591
hg19591
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1647n209
Supporting Variantsnssv17411110
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5896102
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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