A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18181589



Internal ID20748629
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 StatusS
Merged Variantsnsv6446487
Supporting Variants
Samples
Known GenesART1, ART5, CHRNA10, NUP98, TRPC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18181589
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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