A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3738378



Internal ID19036659
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 StatusS
Merged Variantsnsv1009130
Supporting Variants
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)nssv3738378
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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