A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6578007



Internal ID20951078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:23542317..23542849hg38UCSC Ensembl
chr16:23553638..23554170hg19UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg38533
hg19533
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18242681
Samples
Known GenesEARS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6578007
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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