A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6586054



Internal ID20959125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:4448281..4749575hg38UCSC Ensembl
chr16:4498282..4799576hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38301295
hg19301295
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18240637
Samples
Known GenesANKS3, C16orf71, C16orf96, CDIP1, DNAJA3, HMOX2, MGRN1, MIR6769A, NMRAL1, NUDT16L1, UBALD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6586054
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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