A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6553702



Internal ID20926813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:40600839..40601371hg38UCSC Ensembl
chr21:41972766..41973298hg19UCSC Ensembl
Cytoband21q22.2
Allele length
AssemblyAllele length
hg38533
hg19533
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18072748
Samples
Known GenesDSCAM
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6553702
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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