A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17144260



Internal ID21438782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:120669432..120669750hg38UCSC Ensembl
chr8:121681672..121681990hg19UCSC Ensembl
Cytoband8q24.12
Allele length
AssemblyAllele length
hg38319
hg19319
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5582261
Supporting Variants
SamplesHG00732
Known GenesSNTB1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17144260
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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