A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6546719



Internal ID20919929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:43950721..43951207hg38UCSC Ensembl
chr21:45370602..45371088hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38487
hg19487
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18073263
Samples
Known GenesAGPAT3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6546719
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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