A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5887465



Internal ID22662457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:13778445..13782418hg38UCSC Ensembl
chr18:13778444..13782417hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg383974
hg193974
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17477154
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5887465
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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