A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1118080



Internal ID18908225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:128304242..128305626hg38UCSC Ensembl
Outerchr9:131066521..131067905hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg381385
hg191385
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3980296
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1118080
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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