A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1129364



Internal ID19280301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr12:27711862..27719388hg38UCSC Ensembl
Outerchr12:27864795..27872321hg19UCSC Ensembl
Cytoband12p11.22
Allele length
AssemblyAllele length
hg387527
hg197527
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3962801
SamplesKWS1
Known GenesMRPS35
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1129364
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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