A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6597707



Internal ID20970778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:31900629..31901998hg38UCSC Ensembl
chr19:32391535..32392904hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg381370
hg191370
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18245882
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6597707
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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