A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5652171



Internal ID21600476
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:76602139..76602139hg38UCSC Ensembl
chr11:76313183..76313183hg19UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg38201
hg19201
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17076165, nssv17076166
SamplesHG03486, HG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5652171
Frequency
Sample Size35
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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