A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16286634



Internal ID20495852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:27100466..27100466hg38UCSC Ensembl
chr6:27068245..27068245hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg38245
hg19245
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4750565
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16286634
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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