A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1110898



Internal ID19253425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:50278862..50301908hg38UCSC Ensembl
Outerchr13:50852998..50876044hg19UCSC Ensembl
Cytoband13q14.2
Allele length
AssemblyAllele length
hg3823047
hg1923047
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv970n106
Supporting Variantsnssv3961314
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1110898
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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