A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16292013



Internal ID20501231
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:15018722..15018722hg38UCSC Ensembl
chr19:15129534..15129534hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4763814
Supporting Variants
Samples
Known GenesCCDC105
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16292013
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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