A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6570954



Internal ID20944025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:160100807..162576699hg38UCSC Ensembl
chr6:160521839..162997731hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg382475893
hg192475893
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18270497
Samples
Known GenesAGPAT4, AGPAT4-IT1, IGF2R, LPA, LPAL2, MAP3K4, PARK2, PLG, SLC22A1, SLC22A2, SLC22A3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6570954
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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