A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156474



Internal ID22086875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:109700332..109703508hg38UCSC Ensembl
Outerchr1:109697556..109703651hg38UCSC Ensembl
Innerchr1:110242954..110246130hg19UCSC Ensembl
Outerchr1:110240178..110246273hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg386096
hg196096
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv14n97
Supporting Variantsnssv4020425
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156474
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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