A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5875943



Internal ID22650903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:40864965..40866404hg38UCSC Ensembl
chr22:41260969..41262408hg19UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg381440
hg191440
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17483515
Samples
Known GenesXPNPEP3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5875943
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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