A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6589532



Internal ID20962603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:19412936..19413376hg38UCSC Ensembl
chr16:19424258..19424698hg19UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg38441
hg19441
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18239179
Samples
Known GenesTMC5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6589532
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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