A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5876214



Internal ID22651174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:35713662..35716961hg38UCSC Ensembl
chr20:34301584..34304883hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg383300
hg193300
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17485345
Samples
Known GenesRBM39
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5876214
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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