A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17141043



Internal ID21496804
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:109886572..109886572hg38UCSC Ensembl
chr6:110207775..110207775hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38313
hg19313
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5640820
Supporting Variants
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17141043
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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