A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6591624



Internal ID20964695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:428014..744559hg38UCSC Ensembl
chr11:428014..744559hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg38316546
hg19316546
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv928n223
Supporting Variantsnssv18226844
Samples
Known GenesANO9, C11orf35, CDHR5, DEAF1, DRD4, EPS8L2, HRAS, IRF7, LOC143666, LRRC56, MIR210, MIR210HG, PHRF1, PTDSS2, RASSF7, RNH1, SCT, TMEM80
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6591624
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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