A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6577459



Internal ID20950530
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:64563284..64565229hg38UCSC Ensembl
chr15:64855483..64857428hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg381946
hg191946
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18238844
Samples
Known GenesZNF609
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6577459
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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