A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16268777



Internal ID20477995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:152380362..152380362hg38UCSC Ensembl
chr6:152701497..152701497hg19UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg381234
hg191234
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4755506
Supporting Variants
Samples
Known GenesSYNE1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16268777
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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