A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6578503



Internal ID20951574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:50325527..50326685hg38UCSC Ensembl
chr15:50617724..50618882hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg381159
hg191159
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18238089
Samples
Known GenesGABPB1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6578503
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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