A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16273712



Internal ID20482930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:150807049..150807049hg38UCSC Ensembl
chr1:150779525..150779525hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4755068
Supporting Variants
Samples
Known GenesCTSK
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16273712
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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