A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1078301



Internal ID18974035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:117134546..117210021hg38UCSC Ensembl
chr11:117005262..117080737hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3875476
hg1975476
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3765044
SamplesKWP1
Known GenesLOC100652768, PAFAH1B2, PCSK7, SIDT2, TAGLN
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1078301
Frequency
Sample Size1
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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