A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6540356



Internal ID20913647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:32171326..32171963hg38UCSC Ensembl
chr21:33543638..33544275hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg38638
hg19638
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18071926
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6540356
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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