A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4016384



Internal ID22078015
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 Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1155965
Supporting Variants
Samples
Known GenesARHGEF3
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4016384
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer