A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156144



Internal ID22086649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:35898856..35924110hg38UCSC Ensembl
Outerchr4:35898289..35928508hg38UCSC Ensembl
Innerchr4:35900478..35925732hg19UCSC Ensembl
Outerchr4:35899911..35930130hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg3830220
hg1930220
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4014235
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156144
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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