A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1129386



Internal ID18920303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:37265019..37283949hg38UCSC Ensembl
Outerchr18:34844982..34863912hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg3818931
hg1918931
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3962825
SamplesKWS1
Known GenesCELF4
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1129386
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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