A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6594055



Internal ID20967126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:74377295..74378518hg38UCSC Ensembl
chr13:74951432..74952655hg19UCSC Ensembl
Cytoband13q22.1
Allele length
AssemblyAllele length
hg381224
hg191224
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18223229
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6594055
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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