A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1007915



Internal ID18750446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:155758758..155795608hg38UCSC Ensembl
Innerchr3:155476547..155513397hg19UCSC Ensembl
Innerchr3:156959241..156996091hg18UCSC Ensembl
Cytoband3q25.31
Allele length
AssemblyAllele length
hg3836851
hg1936851
hg1836851
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4926n100
Supporting Variantsnssv3606357
Samples
Known GenesC3orf33
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1007915
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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