A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5911211



Internal ID22686424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:20825486..20847840hg38UCSC Ensembl
chr7:20865105..20887459hg19UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg3822355
hg1922355
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17437034
Samples
Known GenesRPL23P8
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5911211
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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