A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6544609



Internal ID20917847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:16793768..16794614hg38UCSC Ensembl
chr21:18166087..18166933hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg38847
hg19847
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18070946
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6544609
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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