A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6595043



Internal ID20968114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:34106939..34137253hg38UCSC Ensembl
chr15:34399140..34429454hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3830315
hg1930315
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18239535
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6595043
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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