A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155965



Internal ID22086470
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:56758727..56764721hg38UCSC Ensembl
Outerchr3:56755924..56769147hg38UCSC Ensembl
Innerchr3:56792755..56798749hg19UCSC Ensembl
Outerchr3:56789952..56803175hg19UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg3813224
hg1913224
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4016384
Samples
Known GenesARHGEF3
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155965
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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