A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17157974



Internal ID21426757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:107107987..107108308hg38UCSC Ensembl
chr8:108120215..108120536hg19UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg38322
hg19322
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5584357
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17157974
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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