A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5911832



Internal ID22687047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:53459446..53459511hg38UCSC Ensembl
chr8:54372006..54372071hg19UCSC Ensembl
Cytoband8q11.23
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17438763
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5911832
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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