A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6579149



Internal ID20952220
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:45483009..45483669hg38UCSC Ensembl
chr15:45775207..45775867hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg38661
hg19661
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18240298
Samples
Known GenesSLC30A4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6579149
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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