A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1120168



Internal ID19282515
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:102423789..102442041hg38UCSC Ensembl
Outerchr8:103436017..103454269hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg3818253
hg1918253
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3960929
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1120168
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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