A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17149813



Internal ID21457024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:113666688..113666688hg38UCSC Ensembl
chr6:113987890..113987890hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5644458
Supporting Variants
SamplesHG02587
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17149813
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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