A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156119



Internal ID22086624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:17542709..17566533hg38UCSC Ensembl
Outerchr4:17540552..17568374hg38UCSC Ensembl
Innerchr4:17544332..17568156hg19UCSC Ensembl
Outerchr4:17542175..17569997hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg3827823
hg1927823
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv214n97
Supporting Variantsnssv4014099
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156119
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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