A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156117



Internal ID22086622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:15758448..15766844hg38UCSC Ensembl
Outerchr4:15758057..15769288hg38UCSC Ensembl
Innerchr4:15760071..15768467hg19UCSC Ensembl
Outerchr4:15759680..15770911hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg3811232
hg1911232
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4014097
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156117
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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