A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15188807



Internal ID21327645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:50212683..50212683hg38UCSC Ensembl
chr22:50651112..50651112hg19UCSC Ensembl
Cytoband22q13.33
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3927589
Supporting Variants
SamplesHG002
Known GenesSELO
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15188807
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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