A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6539389



Internal ID20912687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:31543392..31558004hg38UCSC Ensembl
chr21:32915705..32930317hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg3814613
hg1914613
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18071901
Samples
Known GenesTIAM1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6539389
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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