A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3978634



Internal ID18892190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:389168..574449hg38UCSC Ensembl
Outerchr11:389168..574449hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg38185282
hg19185282
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1116453
Supporting Variants
SamplesKWS2
Known GenesANO9, C11orf35, HRAS, LOC143666, LRRC56, MIR210, MIR210HG, PKP3, PTDSS2, RASSF7, RNH1, SIGIRR
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3978634
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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