A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17072837



Internal ID21407361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:116841749..116842061hg38UCSC Ensembl
chr11:116712465..116712777hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38313
hg19313
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5596226
Supporting Variants
SamplesHG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17072837
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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