A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590729



Internal ID16031452
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:77289437..77295178hg38UCSC Ensembl
Innerchr3:77338588..77344329hg19UCSC Ensembl
Innerchr3:77421278..77427019hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg385742
hg195742
hg185742
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8392n54
Supporting Variantsnssv965821
Samples
Known GenesROBO2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590729
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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