A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1123161



Internal ID18931376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:12664386..12664465hg38UCSC Ensembl
Outerchr18:12664385..12664464hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3972143
SamplesKWS2
Known GenesCEP76, PSMG2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1123161
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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