A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6543249



Internal ID20916501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:26431338..26431945hg38UCSC Ensembl
chr21:27803657..27804264hg19UCSC Ensembl
Cytoband21q21.3
Allele length
AssemblyAllele length
hg38608
hg19608
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18071704
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6543249
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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