A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6540525



Internal ID20913818
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 StatusM
Merged Variants
Supporting Variantsnssv18204142
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)nsv6540525
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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