A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6596378



Internal ID20969449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:45413055..45414185hg38UCSC Ensembl
chr19:45916313..45917443hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg381131
hg191131
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18245645
Samples
Known GenesERCC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6596378
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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