A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5841763



Internal ID22616698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:132171171..132175542hg38UCSC Ensembl
chr5:131506864..131511235hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg384372
hg194372
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17494924
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5841763
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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