A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6335569



Internal ID20868763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:23408237..23414365hg38UCSC Ensembl
chr1:23734730..23740858hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg386129
hg196129
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18202383
Samples
Known GenesTCEA3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6335569
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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