A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14103656



Internal ID21273097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:40472221..40482588hg38UCSC Ensembl
Innerchr22:40868225..40878592hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg3810368
hg1910368
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3110757
Supporting Variants
Samplessample187
Known GenesMKL1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14103656
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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