A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17060069



Internal ID21491959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:100326499..100326499hg38UCSC Ensembl
chr1:100792055..100792055hg19UCSC Ensembl
Cytoband1p21.2
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5619664
Supporting Variants
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17060069
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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