A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5581879



Internal ID21530384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:110930069..110935090hg38UCSC Ensembl
chr1:111472691..111477712hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg385022
hg195022
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17059924
SamplesHG01596
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5581879
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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