A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18071762



Internal ID20638802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:28540301..28541500hg38UCSC Ensembl
chr21:29912623..29913822hg19UCSC Ensembl
Cytoband21q21.3
Allele length
AssemblyAllele length
hg381200
hg191200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6543810
Supporting Variants
Samples
Known GenesLINC00161
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18071762
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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