A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3961264



Internal ID18859257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:389195..574446hg38UCSC Ensembl
Outerchr11:389195..574446hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg38185252
hg19185252
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1110854
Supporting Variants
SamplesKWS1
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)nssv3961264
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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