A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156063



Internal ID22086568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:192529923..192548276hg38UCSC Ensembl
Outerchr3:192526256..192551538hg38UCSC Ensembl
Innerchr3:192247712..192266065hg19UCSC Ensembl
Outerchr3:192244045..192269327hg19UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg3825283
hg1925283
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4017228
Samples
Known GenesFGF12
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156063
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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