A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6446487



Internal ID21104040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:3598372..3731272hg38UCSC Ensembl
chr11:3619602..3752502hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38132901
hg19132901
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv931n223
Supporting Variantsnssv18181589
Samples
Known GenesART1, ART5, CHRNA10, NUP98, TRPC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6446487
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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