A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6585635



Internal ID20958706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:34033887..34034458hg38UCSC Ensembl
chr18:31613851..31614422hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg38572
hg19572
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18244173
Samples
Known GenesNOL4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6585635
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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