A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6444976



Internal ID21102529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:511139..740410hg38UCSC Ensembl
chr11:511139..740410hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg38229272
hg19229272
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18182994
Samples
Known GenesC11orf35, CDHR5, DEAF1, DRD4, EPS8L2, HRAS, IRF7, LOC143666, LRRC56, MIR210, MIR210HG, PHRF1, RASSF7, SCT, TMEM80
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6444976
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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