A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590549



Internal ID16031272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:65861250..65938065hg38UCSC Ensembl
Innerchr3:65846925..65923740hg19UCSC Ensembl
Innerchr3:65821965..65898780hg18UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3876816
hg1976816
hg1876816
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1152485
Samples1780862161_A
Known GenesMAGI1, MAGI1-AS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590549
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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