A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6543852



Internal ID20917093
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 StatusM
Merged Variants
Supporting Variantsnssv18206009
Samples
Known GenesLINC00158
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6543852
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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