A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17645379



Internal ID21837426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:30770181..30770292hg38UCSC Ensembl
chr22:31166168..31166279hg19UCSC Ensembl
Cytoband22q12.2
Allele length
AssemblyAllele length
hg38112
hg19112
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6041889
Supporting Variants
Samples
Known GenesOSBP2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17645379
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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