A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6592477



Internal ID20965548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:87634601..87699935hg38UCSC Ensembl
chr16:87668207..87733541hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg3865335
hg1965335
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18240900
Samples
Known GenesJPH3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6592477
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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