A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6591571



Internal ID20964642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:47840252..47851419hg38UCSC Ensembl
chr15:48132449..48143616hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg3811168
hg1911168
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18238043
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6591571
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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