A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16282318



Internal ID20491536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:49295403..49295403hg38UCSC Ensembl
chr17:47372765..47372765hg19UCSC Ensembl
Cytoband17q21.32
Allele length
AssemblyAllele length
hg38198
hg19198
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4755761
Supporting Variants
Samples
Known GenesZNF652
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16282318
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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