A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17060883



Internal ID21439634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:121257176..121364377hg38UCSC Ensembl
chr1:143985979..144073867hg19UCSC Ensembl
Cytoband1q21.1
Allele length
AssemblyAllele length
hg38107202
hg1987889
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5568772
Supporting Variants
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17060883
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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