A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17076166



Internal ID21477970
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:76602139..76602139hg38UCSC Ensembl
chr11:76313183..76313183hg19UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg38335
hg19335
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5652171
Supporting Variants
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17076166
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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