A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5842809



Internal ID22617744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:57180719..57182618hg38UCSC Ensembl
chr5:56476546..56478445hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg381900
hg191900
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17497421
Samples
Known GenesGPBP1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5842809
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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