A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5881737



Internal ID22656713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:75617571..75620368hg38UCSC Ensembl
chr18:73329526..73332323hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg382798
hg192798
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17479824
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5881737
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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