A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17064965



Internal ID21409903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:29453798..29453798hg38UCSC Ensembl
chr1:29780310..29780310hg19UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5617607
Supporting Variants
SamplesHG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17064965
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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