A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17564480



Internal ID21888835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:92579963..92579963hg38UCSC Ensembl
chr7:92209277..92209277hg19UCSC Ensembl
Cytoband7q21.2
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6079498
Supporting Variants
Samples
Known GenesFAM133B, FAM133DP
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17564480
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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