A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16260929



Internal ID20470147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:39906059..39906059hg38UCSC Ensembl
chr6:39873835..39873835hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4755375
Supporting Variants
Samples
Known GenesMOCS1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16260929
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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