A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5877031



Internal ID22651994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:26195602..26204485hg38UCSC Ensembl
chr18:23775566..23784449hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg388884
hg198884
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17477831
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5877031
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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