A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6584496



Internal ID20957567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:25182952..25184120hg38UCSC Ensembl
chr16:25194273..25195441hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg381169
hg191169
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18242751
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6584496
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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