A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6315833



Internal ID20848907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:159044450..159048622hg38UCSC Ensembl
chr1:159014240..159018412hg19UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg384173
hg194173
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv399n223
Supporting Variantsnssv18200963
Samples
Known GenesIFI16
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6315833
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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