A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6593227



Internal ID20966298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:45246432..45247256hg38UCSC Ensembl
chr13:45820567..45821391hg19UCSC Ensembl
Cytoband13q14.13
Allele length
AssemblyAllele length
hg38825
hg19825
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18234644
Samples
Known GenesGTF2F2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6593227
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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