A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17072662



Internal ID21512382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:101041048..101041048hg38UCSC Ensembl
chr11:100911779..100911779hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg38321
hg19321
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5648860
Supporting Variants
SamplesNA24385
Known GenesPGR
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17072662
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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