A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16270184



Internal ID20479402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:17010524..17010524hg38UCSC Ensembl
chr6:17010755..17010755hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4752625
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16270184
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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