A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6549314



Internal ID20922476
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:30361101..30362900hg38UCSC Ensembl
chr21:31733419..31735218hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg381800
hg191800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18069719
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6549314
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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