A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6579983



Internal ID20953054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:45868340..45869070hg38UCSC Ensembl
chr18:43448305..43449035hg19UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg38731
hg19731
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3359n223
Supporting Variantsnssv18246868
Samples
Known GenesEPG5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6579983
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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