A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16288649



Internal ID20497867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:56264866..56264866hg38UCSC Ensembl
chr5:55560693..55560693hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg3895
hg1995
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4756679
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16288649
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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