A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6560178



Internal ID20933249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:33256824..33257250hg38UCSC Ensembl
chr6:33224601..33225027hg19UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg38427
hg19427
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18271200
Samples
Known GenesVPS52
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6560178
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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