A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1007015



Internal ID18749546
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:53674..1799230hg38UCSC Ensembl
Innerchr3:95357..1840914hg19UCSC Ensembl
Innerchr3:70357..1815914hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg381745557
hg191745558
hg181745558
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4613n100
Supporting Variantsnssv3590262
Samples
Known GenesCHL1, CNTN6
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1007015
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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