A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6453546



Internal ID21111099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:63672701..63673700hg38UCSC Ensembl
chr10:65432461..65433460hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18193120
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6453546
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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