A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1153637



Internal ID18854793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:10609265..12226453hg38UCSC Ensembl
Outerchr18:10609262..12226452hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg381617189
hg191617191
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4002296
SamplesKWB1
Known GenesANKRD62, C18orf61, CHMP1B, GNAL, IMPA2, MIR7153, MPPE1, PIEZO2, SLC35G4
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1153637
Frequency
Sample Size1
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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