A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6596370



Internal ID20969441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:56512444..56575599hg38UCSC Ensembl
chr19:57023813..57086968hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg3863156
hg1963156
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18248509
Samples
Known GenesZFP28, ZNF470, ZNF471
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6596370
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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