A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5880321



Internal ID22655291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:76774321..76774453hg38UCSC Ensembl
chr2:77001447..77001579hg19UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg38133
hg19133
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17404487
Samples
Known GenesLRRTM4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5880321
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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