A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040916



Internal ID18783447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:28270053..28290212hg38UCSC Ensembl
Innerchr10:28558982..28579141hg19UCSC Ensembl
Innerchr10:28598988..28619147hg18UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg3820160
hg1920160
hg1820160
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3506305
Samples
Known GenesMIR8086, MPP7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1040916
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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