A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5911587



Internal ID22686802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:4827318..4827501hg38UCSC Ensembl
chr10:4869510..4869693hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg38184
hg19184
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17355940
Samples
Known GenesAKR1E2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5911587
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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