A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18072347



Internal ID20639387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:38521141..38521815hg38UCSC Ensembl
chr21:39893065..39893739hg19UCSC Ensembl
Cytoband21q22.2
Allele length
AssemblyAllele length
hg38675
hg19675
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6547940
Supporting Variants
Samples
Known GenesERG
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18072347
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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