A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18204142



Internal ID20771182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:44521952..44596004hg38UCSC Ensembl
chr21:45941835..46015895hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3874053
hg1974061
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6540525
Supporting Variants
Samples
Known GenesKRTAP10-1, KRTAP10-2, KRTAP10-3, KRTAP10-4, KRTAP10-5, KRTAP10-6, TSPEAR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18204142
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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