A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1008098



Internal ID18750629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:129558077..129618758hg38UCSC Ensembl
Innerchr3:129276920..129337601hg19UCSC Ensembl
Innerchr3:130759610..130820291hg18UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg3860682
hg1960682
hg1860682
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4859n100
Supporting Variantsnssv3603536, nssv3603535
Samples
Known GenesPLXND1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1008098
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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