A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17139052



Internal ID21411265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:45158837..45161241hg38UCSC Ensembl
chr22:45554718..45557122hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg382405
hg192405
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5590641
Supporting Variants
SamplesHG00513
Known GenesLOC100506714
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17139052
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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