A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17065982



Internal ID21455297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:53443185..53443185hg38UCSC Ensembl
chr1:53908858..53908858hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg38498
hg19498
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5611669
Supporting Variants
SamplesHG02011
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17065982
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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