A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17074816



Internal ID21438313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:58404364..58404364hg38UCSC Ensembl
chr11:58171837..58171837hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg381499
hg191499
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5662730
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17074816
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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