A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5870206



Internal ID22645141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:38034579..38037303hg38UCSC Ensembl
chr20:36662981..36665705hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg382725
hg192725
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17485936
Samples
Known GenesRPRD1B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5870206
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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