A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6580338



Internal ID20953409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:31108008..31109548hg38UCSC Ensembl
chr15:31400211..31401751hg19UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg381541
hg191541
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18239486
Samples
Known GenesTRPM1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6580338
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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