A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6596154



Internal ID20969225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:44978257..44978890hg38UCSC Ensembl
chr19:45481514..45482147hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg38634
hg19634
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18245640
Samples
Known GenesCLPTM1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6596154
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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