A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17071393



Internal ID21471385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:73417831..73418163hg38UCSC Ensembl
chr10:75177589..75177921hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg38333
hg19333
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5603418
Supporting Variants
SamplesHG03125
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17071393
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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