A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6580580



Internal ID20953651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89636100..89730767hg38UCSC Ensembl
chr16:89702508..89797175hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg3894668
hg1994668
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18240915
Samples
Known GenesCDK10, CHMP1A, DPEP1, SPATA2L, SPATA33, VPS9D1, VPS9D1-AS1, ZNF276
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6580580
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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