A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5888096



Internal ID22663097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:23889688..23950802hg38UCSC Ensembl
chr6:23889916..23951030hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3861115
hg1961115
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17442765
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5888096
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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