A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6540249



Internal ID20913541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:33537301..33561500hg38UCSC Ensembl
chr21:34909607..34933806hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg3824200
hg1924200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18206667
Samples
Known GenesGART, MIR6501, SON
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6540249
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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