A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6590974



Internal ID20964045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:70883232..70884523hg38UCSC Ensembl
chr15:71175571..71176862hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg381292
hg191292
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18239653
Samples
Known GenesLRRC49, THAP10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6590974
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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