A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6557804



Internal ID20930875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:73477017..73477374hg38UCSC Ensembl
chr6:74186740..74187097hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg38358
hg19358
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18274096
Samples
Known GenesMTO1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6557804
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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