A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6594605



Internal ID20967676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:14764459..14765293hg38UCSC Ensembl
chr18:14764458..14765292hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg38835
hg19835
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18244111
Samples
Known GenesANKRD30B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6594605
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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