A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6455207



Internal ID21112760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:28682408..28704680hg38UCSC Ensembl
chr10:28971337..28993609hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3822273
hg1922273
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18196517
Samples
Known GenesBAMBI
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6455207
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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