A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5879352



Internal ID22654321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:31463142..31512067hg38UCSC Ensembl
chr20:30050945..30099870hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg3848926
hg1948926
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17485268
Samples
Known GenesDEFB124, LINC00028, REM1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5879352
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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