A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1129411



Internal ID18916835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:38357657..38358216hg38UCSC Ensembl
Outerchr3:38399148..38399707hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg38560
hg19560
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3962853
SamplesKWS1
Known GenesXYLB
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1129411
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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