A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6538250



Internal ID20911571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:46428263..46453759hg38UCSC Ensembl
chr21:47848177..47873672hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3825497
hg1925496
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18204212
Samples
Known GenesPCNT
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6538250
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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