A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6594536



Internal ID20967607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:96258459..96258602hg38UCSC Ensembl
chr15:96801688..96801831hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg38144
hg19144
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18239112
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6594536
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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