A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6316449



Internal ID20849528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:109571897..109573694hg38UCSC Ensembl
chr1:110114519..110116316hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg381798
hg191798
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18199244
Samples
Known GenesGNAI3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6316449
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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