A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6078766



Internal ID21987999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:16266435..16266435hg38UCSC Ensembl
chr6:16266666..16266666hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3896
hg1996
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17559005
Samples
Known GenesGMPR
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6078766
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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