A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590363



Internal ID16031086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:56952459..56978210hg38UCSC Ensembl
Innerchr3:56986487..57012238hg19UCSC Ensembl
Innerchr3:56961527..56987278hg18UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg3825752
hg1925752
hg1825752
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv963362
Samples
Known GenesARHGEF3, ARHGEF3-AS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590363
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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