A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037911



Internal ID19127130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:105342384..105557234hg38UCSC Ensembl
Innerchr10:107102142..107316992hg19UCSC Ensembl
Innerchr10:107092132..107306982hg18UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg38214851
hg19214851
hg18214851
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv968n100
Supporting Variantsnssv3706216, nssv3512095, nssv3520772, nssv3513269, nssv3521676
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1037911
Frequency
Sample Size11257
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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