A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18069871



Internal ID20636911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:20246995..20247309hg38UCSC Ensembl
chr21:21619308..21619622hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg38315
hg19315
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6538340
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18069871
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00077


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