A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17075551



Internal ID21440582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:59672310..59672375hg38UCSC Ensembl
chr11:59439783..59439848hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5595698
Supporting Variants
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17075551
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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