A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6592296



Internal ID20965367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:645737..844243hg38UCSC Ensembl
chr18:645737..844244hg19UCSC Ensembl
Cytoband18p11.32
Allele length
AssemblyAllele length
hg38198507
hg19198508
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18245490
Samples
Known GenesC18orf56, CLUL1, ENOSF1, TYMS, YES1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6592296
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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