A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1007766



Internal ID19096985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:17266821..17296402hg38UCSC Ensembl
Innerchr1:17593316..17622897hg19UCSC Ensembl
Innerchr1:17465903..17495484hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3829582
hg1929582
hg1829582
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv129n100
Supporting Variantsnssv3700286
Samples
Known GenesPADI3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1007766
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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