A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1006307



Internal ID19095525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:173912878..173983742hg38UCSC Ensembl
Innerchr3:173630668..173701532hg19UCSC Ensembl
Innerchr3:175113362..175184226hg18UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg3870865
hg1970865
hg1870865
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4987n100
Supporting Variantsnssv3613616
Samples
Known GenesNLGN1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1006307
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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