A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17059924



Internal ID21451959
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 StatusS
Merged Variantsnsv5581879
Supporting Variants
SamplesHG01596
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17059924
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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