A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18068664



Internal ID20635704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:14839819..14847817hg38UCSC Ensembl
chr21:16212140..16220138hg19UCSC Ensembl
Cytoband21q11.2
Allele length
AssemblyAllele length
hg387999
hg197999
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6539868
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18068664
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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