A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1125442



Internal ID19284667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:102311387..102317863hg38UCSC Ensembl
Outerchr9:105073669..105080145hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg386477
hg196477
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3983615
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1125442
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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