A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6584072



Internal ID20957143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:14685412..14685815hg38UCSC Ensembl
chr16:14779269..14779672hg19UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg38404
hg19404
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2696n223
Supporting Variantsnssv18239952
Samples
Known GenesPLA2G10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6584072
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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