A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6585719



Internal ID20958790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:23517960..23518308hg38UCSC Ensembl
chr18:21097924..21098272hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg38349
hg19349
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18246785
Samples
Known GenesC18orf8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6585719
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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