A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17064748



Internal ID21464584
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:32408713..32409813hg38UCSC Ensembl
chr1:32874314..32875414hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg381101
hg191101
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5578463
Supporting Variants
SamplesHG03065
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17064748
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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