A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1145908



Internal ID18856666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:37338044..37338338hg38UCSC Ensembl
Outerchr18:34918007..34918301hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg38295
hg19295
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3997269
SamplesKWB1
Known GenesCELF4
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1145908
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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