A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5868162



Internal ID22643097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:43104419..43114737hg38UCSC Ensembl
chr22:43500425..43510743hg19UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg3810319
hg1910319
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17483625
Samples
Known GenesBIK
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5868162
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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