A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17152066



Internal ID21457074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:73433229..73436609hg38UCSC Ensembl
chr8:74345464..74348844hg19UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg383381
hg193381
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5565845
Supporting Variants
SamplesHG02587
Known GenesSTAU2, STAU2-AS1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17152066
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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