A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18206009



Internal ID20773049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:25215358..25420517hg38UCSC Ensembl
chr21:26587672..26792829hg19UCSC Ensembl
Cytoband21q21.2
Allele length
AssemblyAllele length
hg38205160
hg19205158
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6543852
Supporting Variants
Samples
Known GenesLINC00158
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18206009
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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