A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6561159



Internal ID20934230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:73476978..73477213hg38UCSC Ensembl
chr6:74186701..74186936hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg38236
hg19236
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18274095
Samples
Known GenesMTO1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6561159
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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