A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5881750



Internal ID22656726
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:31387349..31446696hg38UCSC Ensembl
chr20:29975152..30034499hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg3859348
hg1959348
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17485257
Samples
Known GenesDEFB119, DEFB121, DEFB122, DEFB123
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5881750
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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