A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17153208



Internal ID21453884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:11801342..11801342hg38UCSC Ensembl
chr6:11801575..11801575hg19UCSC Ensembl
Cytoband6p24.1
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5628323
Supporting Variants
SamplesHG02011
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17153208
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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