A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6546233



Internal ID20919452
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:38539669..38545155hg38UCSC Ensembl
chr21:39911593..39917079hg19UCSC Ensembl
Cytoband21q22.2
Allele length
AssemblyAllele length
hg385487
hg195487
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18072349
Samples
Known GenesERG
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6546233
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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