A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6552005



Internal ID20925136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:32720165..32722140hg38UCSC Ensembl
chr21:34092475..34094450hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg381976
hg191976
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18206658
Samples
Known GenesSYNJ1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6552005
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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