A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14102774



Internal ID21267330
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:45139789..45144847hg38UCSC Ensembl
Innerchr22:45535670..45540728hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg385059
hg195059
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3110634
Supporting Variants
Samplessample111
Known GenesLOC100506714
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14102774
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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