A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17068496



Internal ID21506269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:103909392..103909443hg38UCSC Ensembl
chr10:105669150..105669201hg19UCSC Ensembl
Cytoband10q24.33
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5597173
Supporting Variants
SamplesNA19983
Known GenesOBFC1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17068496
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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