A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5875451



Internal ID22650408
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:37247139..37252027hg38UCSC Ensembl
chr22:37643179..37648067hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg384889
hg194889
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17482936
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5875451
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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