A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17072200



Internal ID21470612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:118862540..118862709hg38UCSC Ensembl
chr11:118733249..118733418hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38170
hg19170
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5603207
Supporting Variants
SamplesHG03125
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17072200
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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