A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17156701



Internal ID21473329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:98941311..98943180hg38UCSC Ensembl
chr6:99389187..99391056hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg381870
hg191870
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5579436
Supporting Variants
SamplesHG03371
Known GenesFBXL4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17156701
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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