A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5841574



Internal ID22616509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:171047756..171111290hg38UCSC Ensembl
chr5:170474760..170538294hg19UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg3863535
hg1963535
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17497688
Samples
Known GenesRANBP17
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5841574
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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