A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5646007



Internal ID21594312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:31213100..31213100hg38UCSC Ensembl
chr11:31234647..31234647hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38402
hg19402
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17073949, nssv17073948
SamplesHG03486, HG00171
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5646007
Frequency
Sample Size35
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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