A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6596780



Internal ID20969851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:6136151..6140238hg38UCSC Ensembl
chr19:6136162..6140249hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg384088
hg194088
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18249146
Samples
Known GenesACSBG2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6596780
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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