A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17500032



Internal ID22557968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:98941333..98943232hg38UCSC Ensembl
chr6:99389209..99391108hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg381900
hg191900
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5845862
Supporting Variants
Samples
Known GenesFBXL4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17500032
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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