A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6594998



Internal ID20968069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:24710151..24710781hg38UCSC Ensembl
chr16:24721472..24722102hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg38631
hg19631
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18242729
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6594998
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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