A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1129378



Internal ID19260890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:38624426..38624491hg38UCSC Ensembl
Outerchr15:38916627..38916692hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3962817
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1129378
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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