A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590731



Internal ID16031454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:77290005..77295633hg38UCSC Ensembl
Innerchr3:77339156..77344784hg19UCSC Ensembl
Innerchr3:77421846..77427474hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg385629
hg195629
hg185629
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8392n54
Supporting Variantsnssv965824
Samples
Known GenesROBO2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590731
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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