A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046887



Internal ID19136106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:82650973..82670651hg38UCSC Ensembl
Innerchr10:84410729..84430407hg19UCSC Ensembl
Innerchr10:84400709..84420387hg18UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg3819679
hg1919679
hg1819679
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv945n100
Supporting Variantsnssv3509343
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)nsv1046887
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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