A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15189984



Internal ID21328829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:39698775..39698775hg38UCSC Ensembl
chr22:40094780..40094780hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3941146
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15189984
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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