A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16290662



Internal ID20499880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:47740516..47740516hg38UCSC Ensembl
chr6:47708252..47708252hg19UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg38330
hg19330
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4765854
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16290662
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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