A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6581132



Internal ID20954203
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:3572999..3574008hg38UCSC Ensembl
chr16:3623000..3624009hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg381010
hg191010
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2662n223
Supporting Variantsnssv18239991
Samples
Known GenesNLRC3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6581132
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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