A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17139619



Internal ID21411737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:81334368..81334466hg38UCSC Ensembl
chr8:82246603..82246701hg19UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg3899
hg1999
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5578483
Supporting Variants
SamplesHG00513
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17139619
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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