A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6592138



Internal ID20965209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:88026108..88027482hg38UCSC Ensembl
chr15:88569339..88570713hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg381375
hg191375
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18240524
Samples
Known GenesNTRK3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6592138
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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