A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17076442



Internal ID21459123
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:93535787..93535787hg38UCSC Ensembl
chr11:93268953..93268953hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg38186
hg19186
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5658249
Supporting Variants
SamplesHG02818
Known GenesSMCO4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17076442
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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