A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6596708



Internal ID20969779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:53092322..53093445hg38UCSC Ensembl
chr19:53595575..53596698hg19UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg381124
hg191124
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18246748
Samples
Known GenesZNF160
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6596708
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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