A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17063327



Internal ID21469498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:23710865..23710865hg38UCSC Ensembl
chr1:24037355..24037355hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38549
hg19549
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5605927
Supporting Variants
SamplesHG03125
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17063327
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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