A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5842753



Internal ID22617688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:50530040..50540729hg38UCSC Ensembl
chr5:49825874..49836563hg19UCSC Ensembl
Cytoband5q11.1
Allele length
AssemblyAllele length
hg3810690
hg1910690
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17497331
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5842753
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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