A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6585584



Internal ID20958655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:3134944..5291746hg38UCSC Ensembl
chr18:3134942..5291745hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg382156803
hg192156804
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18244025
Samples
Known GenesC18orf42, DLGAP1, DLGAP1-AS1, DLGAP1-AS3, DLGAP1-AS4, DLGAP1-AS5, LINC00526, LINC00667, MIR6718, MYL12A, MYL12B, MYOM1, TGIF1, ZBTB14
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6585584
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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