A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17062337



Internal ID21401980
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:198034476..198037885hg38UCSC Ensembl
chr1:198003606..198007015hg19UCSC Ensembl
Cytoband1q31.3
Allele length
AssemblyAllele length
hg383410
hg193410
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5573545
Supporting Variants
SamplesHG00096
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17062337
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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