A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16277174



Internal ID20486392
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:152609444..152609444hg38UCSC Ensembl
chr5:151989004..151989004hg19UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4753335
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16277174
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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