A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1141890



Internal ID18914896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:121193584..121858337hg38UCSC Ensembl
Outerchr3:120912431..121577184hg19UCSC Ensembl
Cytoband3q13.33
Allele length
AssemblyAllele length
hg38664754
hg19664754
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3993397
SamplesKWS2
Known GenesARGFX, EAF2, FBXO40, GOLGB1, HCLS1, IQCB1, POLQ, STXBP5L
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1141890
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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