A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1111733



Internal ID18913590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:18597152..18598438hg38UCSC Ensembl
Outerchr8:18454662..18455948hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg381287
hg191287
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3789n106
Supporting Variantsnssv3964636
SamplesKWS2
Known GenesPSD3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1111733
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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