A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15706691



Internal ID21378967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:38363805..38363896hg38UCSC Ensembl
chr22:38759810..38759901hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg3892
hg1992
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4392820
Supporting Variants
Samples
Known GenesLOC400927
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nssv15706691
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0229885


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