A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5877140



Internal ID22652103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:37047728..37050227hg38UCSC Ensembl
chr20:35676131..35678630hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg382500
hg192500
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17485378
Samples
Known GenesRBL1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5877140
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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