A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6544783



Internal ID20918020
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:19130262..19130679hg38UCSC Ensembl
chr21:20502580..20502997hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg38418
hg19418
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18070725
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6544783
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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