A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5876726



Internal ID22651687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:50725256..50729055hg38UCSC Ensembl
chr22:51163684..51167483hg19UCSC Ensembl
Cytoband22q13.33
Allele length
AssemblyAllele length
hg383800
hg193800
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17484333
Samples
Known GenesSHANK3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5876726
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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