A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6594494



Internal ID20967565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:64653522..64654325hg38UCSC Ensembl
chr15:64945721..64946524hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38804
hg19804
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18238850
Samples
Known GenesZNF609
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6594494
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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