A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17145510



Internal ID21421369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:17127475..17127535hg38UCSC Ensembl
chr8:16984984..16985044hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5582661
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17145510
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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