A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6599180



Internal ID20972251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:6154136..6154574hg38UCSC Ensembl
chr19:6154147..6154585hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38439
hg19439
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18249147
Samples
Known GenesACSBG2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6599180
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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