A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17076279



Internal ID21413636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:83714212..83714212hg38UCSC Ensembl
chr11:83425255..83425255hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38356
hg19356
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5645247
Supporting Variants
SamplesHG00513
Known GenesDLG2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17076279
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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