A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6582340



Internal ID20955411
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:28016840..28019821hg38UCSC Ensembl
chr16:28028161..28031142hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg382982
hg192982
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18242821
Samples
Known GenesGSG1L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6582340
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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