A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6560268



Internal ID20933339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:160148869..160149594hg38UCSC Ensembl
chr6:160569901..160570626hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg38726
hg19726
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18270500
Samples
Known GenesSLC22A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6560268
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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