A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15179539



Internal ID21318335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:47260818..47260890hg38UCSC Ensembl
chr22:47656568..47656640hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3937158
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15179539
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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