A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6585393



Internal ID20958464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:26590885..26591861hg38UCSC Ensembl
chr18:24170849..24171825hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg38977
hg19977
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3330n223
Supporting Variantsnssv18243949
Samples
Known GenesKCTD1, MIR8057
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6585393
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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