A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046193



Internal ID18788724
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46203032..46281567hg38UCSC Ensembl
Innerchr10:47574268..47652803hg19UCSC Ensembl
Innerchr10:47044274..47122809hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3878536
hg1978536
hg1878536
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv840n100
Supporting Variantsnssv3706817
Samples
Known GenesANTXRLP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1046193
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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