A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6554399



Internal ID20927495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:42349287..42349387hg38UCSC Ensembl
chr21:43769396..43769496hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38101
hg19101
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18072470
Samples
Known GenesTFF2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6554399
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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