A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17145302



Internal ID21404250
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:16266338..16266390hg38UCSC Ensembl
chr6:16266569..16266621hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5579499
Supporting Variants
SamplesHG00512
Known GenesGMPR
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17145302
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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