A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6596229



Internal ID20969300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:33158400..33171455hg38UCSC Ensembl
chr19:33649306..33662361hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg3813056
hg1913056
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18245929
Samples
Known GenesWDR88
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6596229
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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