A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5875625



Internal ID22650583
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:26205061..26208824hg38UCSC Ensembl
chr18:23785025..23788788hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg383764
hg193764
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17477832
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5875625
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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