A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1110904



Internal ID19247998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:85586219..85592309hg38UCSC Ensembl
Outerchr13:86160354..86166444hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg386091
hg196091
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3961320
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1110904
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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