A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046146



Internal ID18788677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46215430..46332377hg38UCSC Ensembl
Innerchr10:47586666..47703613hg19UCSC Ensembl
Innerchr10:47056672..47173619hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38116948
hg19116948
hg18116948
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv843n100
Supporting Variantsnssv3514761, nssv3520424
Samples
Known GenesANTXRL, ANTXRLP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1046146
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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