A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16266377



Internal ID20475595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:41771555..41771555hg38UCSC Ensembl
chr17:39927807..39927807hg19UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4760572
Supporting Variants
Samples
Known GenesJUP
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16266377
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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