A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6576268



Internal ID20949339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:76227107..76228489hg38UCSC Ensembl
chr15:76519448..76520830hg19UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg381383
hg191383
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18242009
Samples
Known GenesETFA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6576268
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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