A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17154196



Internal ID21481838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:123052748..123053078hg38UCSC Ensembl
chr6:123373893..123374223hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg38331
hg19331
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5577435
Supporting Variants
SamplesHG03683
Known GenesCLVS2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17154196
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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