A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6553293



Internal ID20926402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:41185074..41185563hg38UCSC Ensembl
chr21:42557001..42557490hg19UCSC Ensembl
Cytoband21q22.2
Allele length
AssemblyAllele length
hg38490
hg19490
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18071470
Samples
Known GenesBACE2, PLAC4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6553293
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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