A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17076286



Internal ID21415675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:84099840..84099840hg38UCSC Ensembl
chr11:83810883..83810883hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38110
hg19110
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5658296
Supporting Variants
SamplesHG00731
Known GenesDLG2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17076286
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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