A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6544932



Internal ID20918170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:46193601..46196000hg38UCSC Ensembl
chr21:47613515..47615914hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg382400
hg192400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18204203
Samples
Known GenesLSS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6544932
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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