A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6333435



Internal ID20866611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:153754820..153756666hg38UCSC Ensembl
chr1:153727296..153729142hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg381847
hg191847
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18200494
Samples
Known GenesINTS3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6333435
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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