A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1110981



Internal ID19254295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:144682140..144695220hg38UCSC Ensembl
Outerchr8:145907525..145920605hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3813081
hg1913081
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3961410
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1110981
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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