A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5658897



Internal ID21607202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:36507572..36507572hg38UCSC Ensembl
chr11:36529122..36529122hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg38262
hg19262
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17074579
SamplesHG00731
Known GenesTRAF6
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5658897
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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