A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6591350



Internal ID20964421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:19630423..19631074hg38UCSC Ensembl
chr16:19641745..19642396hg19UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg38652
hg19652
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18239191
Samples
Known GenesC16orf62
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6591350
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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