A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17146514



Internal ID21477595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:41757790..41757867hg38UCSC Ensembl
chr6:41725528..41725605hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5580981
Supporting Variants
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17146514
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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