A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16287645



Internal ID20496863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:24917383..24917383hg38UCSC Ensembl
chr7:24957002..24957002hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4761993
Supporting Variants
Samples
Known GenesOSBPL3
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16287645
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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