A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6576825



Internal ID20949896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:41305850..41458981hg38UCSC Ensembl
chr15:41598048..41751179hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38153132
hg19153132
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18238323
Samples
Known GenesNDUFAF1, NUSAP1, OIP5, RTF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6576825
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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