A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5875105



Internal ID22650060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:47804971..47806315hg38UCSC Ensembl
chr20:46433715..46435059hg19UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg381345
hg191345
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17486080
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5875105
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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