A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1150503



Internal ID19197851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:57278290..57278374hg38UCSC Ensembl
Outerchr18:54945521..54945605hg19UCSC Ensembl
Cytoband18q21.31
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3995970
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1150503
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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