A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv945n100



Internal ID22787032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:82650973..82677437hg38UCSC Ensembl
chr10:84410729..84437193hg19UCSC Ensembl
chr10:84400709..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 Variants
Supporting Variantsnsv1037361, nsv1050478, nsv1048978, nsv1045391, nsv1053404, nsv1040748, nsv1048768, nsv1046887, nsv1042480
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)dgv945n100
Frequency
Sample Size11257
Observed Gain52
Observed Loss0
Observed Complex0
Frequencyn/a


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