A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156473



Internal ID22086874
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:109700332..109702376hg38UCSC Ensembl
Outerchr1:109697556..109703504hg38UCSC Ensembl
Innerchr1:110242954..110244998hg19UCSC Ensembl
Outerchr1:110240178..110246126hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg385949
hg195949
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv14n97
Supporting Variantsnssv4020424, nssv4020422, nssv4020421, nssv4020423
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156473
Frequency
Sample Size131
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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