A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6579495



Internal ID20952566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:44983238..44983745hg38UCSC Ensembl
chr13:45557373..45557880hg19UCSC Ensembl
Cytoband13q14.12
Allele length
AssemblyAllele length
hg38508
hg19508
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18235470
Samples
Known GenesNUFIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6579495
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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