A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6595017



Internal ID20968088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:40817344..40817653hg38UCSC Ensembl
chr15:41109542..41109851hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38310
hg19310
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18238278
Samples
Known GenesPPP1R14D
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6595017
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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