A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6453531



Internal ID21111084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:114045701..114049600hg38UCSC Ensembl
chr10:115805460..115809359hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg383900
hg193900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18188416
Samples
Known GenesADRB1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6453531
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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