A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1048768



Internal ID19137987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:82650973..82672587hg38UCSC Ensembl
Innerchr10:84410729..84432343hg19UCSC Ensembl
Innerchr10:84400709..84422323hg18UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg3821615
hg1921615
hg1821615
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv945n100
Supporting Variantsnssv3506348, nssv3522689, nssv3706183, nssv3505858
Samples
Known GenesNRG3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1048768
Frequency
Sample Size11257
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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