A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17152001



Internal ID21503573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:35501540..35501623hg38UCSC Ensembl
chr6:35469317..35469400hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5566435
Supporting Variants
SamplesNA19239
Known GenesTULP1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17152001
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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