A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5573936



Internal ID21522345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:69626119..69626235hg38UCSC Ensembl
chr8:70538354..70538470hg19UCSC Ensembl
Cytoband8q13.3
Allele length
AssemblyAllele length
hg38117
hg19117
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17155339
SamplesHG00731
Known GenesSULF1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5573936
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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