A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1151090



Internal ID18848914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:11826179..11826506hg38UCSC Ensembl
Outerchr18:11826178..11826505hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg38328
hg19328
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4002022
SamplesKWB1
Known GenesGNAL
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1151090
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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