A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154975



Internal ID22085480
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:113454537..113458073hg38UCSC Ensembl
Outerchr13:113452519..113459919hg38UCSC Ensembl
Innerchr13:114108852..114112388hg19UCSC Ensembl
Outerchr13:114106834..114114234hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg387401
hg197401
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4008313
Samples
Known GenesADPRHL1, DCUN1D2
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154975
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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