A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6584718



Internal ID20957789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:57982832..57983626hg38UCSC Ensembl
chr16:58016736..58017530hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38795
hg19795
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18239328
Samples
Known GenesTEPP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6584718
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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