A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1125397



Internal ID19274009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:39469255..39469310hg38UCSC Ensembl
Outerchr3:39510746..39510801hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3983568
SamplesKWS2
Known GenesMOBP
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1125397
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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