A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009130



Internal ID19098348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:173907550..173993420hg38UCSC Ensembl
Innerchr3:173625340..173711210hg19UCSC Ensembl
Innerchr3:175108034..175193904hg18UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg3885871
hg1985871
hg1885871
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4987n100
Supporting Variantsnssv3738378
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)nsv1009130
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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