A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1077764



Internal ID18971239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:389389..574439hg38UCSC Ensembl
chr11:389389..574439hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg38185051
hg19185051
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3772166
SamplesKWP1
Known GenesANO9, C11orf35, HRAS, LOC143666, LRRC56, MIR210, MIR210HG, PKP3, PTDSS2, RASSF7, RNH1, SIGIRR
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1077764
Frequency
Sample Size1
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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