A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18239653



Internal ID20806693
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 StatusS
Merged Variantsnsv6590974
Supporting Variants
Samples
Known GenesLRRC49, THAP10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18239653
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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