A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040748



Internal ID19129967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:82650973..82677437hg38UCSC Ensembl
Innerchr10:84410729..84437193hg19UCSC Ensembl
Innerchr10:84400709..84427173hg18UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg3826465
hg1926465
hg1826465
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv945n100
Supporting Variantsnssv3506130
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)nsv1040748
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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