A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5893239



Internal ID22668298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:11996627..11999450hg38UCSC Ensembl
chr6:11996860..11999683hg19UCSC Ensembl
Cytoband6p24.1
Allele length
AssemblyAllele length
hg382824
hg192824
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17423425
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5893239
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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