A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1118240



Internal ID19252458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:9385391..9385732hg38UCSC Ensembl
Outerchr18:9385389..9385730hg19UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg38342
hg19342
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1546n106
Supporting Variantsnssv3980911
SamplesKWS1
Known GenesTWSG1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1118240
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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