A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044184



Internal ID19133403
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:93120446..93151543hg38UCSC Ensembl
Innerchr10:94880203..94911300hg19UCSC Ensembl
Innerchr10:94870193..94901290hg18UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg3831098
hg1931098
hg1831098
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3706194
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)nsv1044184
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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