A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4987n100



Internal ID22791074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:173907550..173993420hg38UCSC Ensembl
chr3:173625340..173711210hg19UCSC Ensembl
chr3:175108034..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 Variants
Supporting Variantsnsv1009130, nsv1006307
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)dgv4987n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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