A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6553494



Internal ID20926603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:32515317..32534900hg38UCSC Ensembl
chr21:33887627..33907210hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg3819584
hg1919584
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18071935
Samples
Known GenesEVA1C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6553494
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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