A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17140554



Internal ID21479256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:151669147..151669147hg38UCSC Ensembl
chr6:151990282..151990282hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5637994
Supporting Variants
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17140554
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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