A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17061469



Internal ID21432524
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:185403964..185404301hg38UCSC Ensembl
chr1:185373096..185373433hg19UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg38338
hg19338
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5568087
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17061469
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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