A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16282749



Internal ID20491967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:152139686..152139686hg38UCSC Ensembl
chr6:152460821..152460821hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4751273
Supporting Variants
Samples
Known GenesSYNE1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16282749
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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