A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045391



Internal ID19134610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:82650973..82672072hg38UCSC Ensembl
Innerchr10:84410729..84431828hg19UCSC Ensembl
Innerchr10:84400709..84421808hg18UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg3821100
hg1921100
hg1821100
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv945n100
Supporting Variantsnssv3519426, nssv3706182, nssv3514436, nssv3509344, nssv3517411, nssv3514747, nssv3706181
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)nsv1045391
Frequency
Sample Size11257
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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