A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6565072



Internal ID20938143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:11964842..17051222hg38UCSC Ensembl
chr6:11965075..17051453hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg385086381
hg195086379
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18268617
Samples
Known GenesATXN1, CD83, DTNBP1, EDN1, GFOD1, GMPR, HIVEP1, JARID2, LINC01108, LOC100130357, MCUR1, MIR4639, MYLIP, NOL7, PHACTR1, RANBP9, RNF182, RNU6-48P, SIRT5, TBC1D7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6565072
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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