A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6071891



Internal ID21981124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:112317998..112317998hg38UCSC Ensembl
chr8:113330227..113330227hg19UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17591240
Samples
Known GenesCSMD3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6071891
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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