A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5842811



Internal ID22617746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:57897482..57899814hg38UCSC Ensembl
chr5:57193309..57195641hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg382333
hg192333
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1692n209
Supporting Variantsnssv17497425, nssv17499864
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5842811
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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