A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16284155



Internal ID20493373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:6101613..6101613hg38UCSC Ensembl
chr5:6101726..6101726hg19UCSC Ensembl
Cytoband5p15.32
Allele length
AssemblyAllele length
hg38170
hg19170
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4763897
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16284155
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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