A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16287927



Internal ID20497145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:73506928..73506928hg38UCSC Ensembl
chr6:74216651..74216651hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg38688
hg19688
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4764305
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16287927
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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