A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6546327



Internal ID20919545
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:36019282..36037294hg38UCSC Ensembl
chr21:37391580..37409592hg19UCSC Ensembl
Cytoband21q22.12
Allele length
AssemblyAllele length
hg3818013
hg1918013
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203937
Samples
Known GenesSETD4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6546327
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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