A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5890966



Internal ID22665998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:76812308..76832686hg38UCSC Ensembl
chr5:76108133..76128511hg19UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg3820379
hg1920379
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17410664
Samples
Known GenesF2RL1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5890966
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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