A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5841657



Internal ID22616592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:131038886..131103185hg38UCSC Ensembl
chr5:130374579..130438878hg19UCSC Ensembl
Cytoband5q23.3
Allele length
AssemblyAllele length
hg3864300
hg1964300
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17494895
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5841657
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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