A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17064289



Internal ID21478809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:25767731..25767920hg38UCSC Ensembl
chr1:26094222..26094411hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38190
hg19190
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5566221
Supporting Variants
SamplesHG03486
Known GenesMAN1C1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17064289
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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