A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6057652



Internal ID21966885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:31591702..31591825hg38UCSC Ensembl
chr22:31987688..31987811hg19UCSC Ensembl
Cytoband22q12.2
Allele length
AssemblyAllele length
hg38124
hg19124
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17638159
Samples
Known GenesSFI1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6057652
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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