A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6439780



Internal ID21097333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:3562701..3708100hg38UCSC Ensembl
chr11:3583931..3729330hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38145400
hg19145400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv931n223
Supporting Variantsnssv18183018
Samples
Known GenesART1, ART5, CHRNA10, NUP98, TRPC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6439780
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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