A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6555471



Internal ID20928558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:18685001..18712400hg38UCSC Ensembl
chr21:20057319..20084718hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg3827400
hg1927400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18070667
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6555471
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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