A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17156522



Internal ID21494328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:142500220..142500220hg38UCSC Ensembl
chr8:143581581..143581581hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5635946
Supporting Variants
SamplesNA19238
Known GenesBAI1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17156522
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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