A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16295630



Internal ID20504848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:4254614..4254614hg38UCSC Ensembl
chr6:4254848..4254848hg19UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg38121
hg19121
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4762341
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16295630
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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