A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5843908



Internal ID22618843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:95950664..95966320hg38UCSC Ensembl
chr5:95286368..95302024hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg3815657
hg1915657
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17500122
Samples
Known GenesELL2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5843908
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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