A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17641632



Internal ID21833679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:45315635..45315702hg38UCSC Ensembl
chr22:45711516..45711583hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6045484
Supporting Variants
Samples
Known GenesFAM118A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17641632
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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