A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6546297



Internal ID20919515
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:26091540..26094897hg38UCSC Ensembl
chr21:27463856..27467214hg19UCSC Ensembl
Cytoband21q21.3
Allele length
AssemblyAllele length
hg383358
hg193359
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18071684
Samples
Known GenesAPP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6546297
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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