A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17146869



Internal ID21465022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:113441184..113441184hg38UCSC Ensembl
chr6:113762386..113762386hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5639723
Supporting Variants
SamplesHG03065
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17146869
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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