A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16263374



Internal ID20472592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:32948010..32948010hg38UCSC Ensembl
chr17:31275028..31275028hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4766927
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16263374
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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