A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6552201



Internal ID20925329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:19045791..19049883hg38UCSC Ensembl
chr21:20418110..20422202hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg384093
hg194093
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18070717
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6552201
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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