A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156250



Internal ID22086755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:157808407..157810226hg38UCSC Ensembl
Outerchr4:157808285..157815297hg38UCSC Ensembl
Innerchr4:158729559..158731378hg19UCSC Ensembl
Outerchr4:158729437..158736449hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg387013
hg197013
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4015726, nssv4015727
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156250
Frequency
Sample Size131
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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