A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5876707



Internal ID22651668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:37043157..37044575hg38UCSC Ensembl
chr20:35671560..35672978hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg381419
hg191419
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17485376, nssv17485377
Samples
Known GenesRBL1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5876707
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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